=== h04_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h05_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h06_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h08_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h09_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h10_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h11_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h15_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h21_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h22_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h27_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h28_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h33_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h34_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h35_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h37_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h39_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h40_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h42_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h43_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h45_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h47_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h48_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h49_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h51_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h52_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h53_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h57_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h59_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h61_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h62_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h63_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h64_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h65_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h69_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h73_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h74_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h91_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight from "guilt-by-association" rescue === h92_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight from "guilt-by-association" rescue === h93_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === h95ctrls_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight computed with the 'rescue' strategy ( Faulkner et al. Genomics. 2008 91:281 ) === i02_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight from "guilt-by-association" rescue === i03_mapping.tbl.txt.bz2 ##ColumnVariable[id] = extracted tag sequence ##ColumnVariable[library_count] = read count in this library. SUM( rna_count ) = library_count ##ColumnVariable[edit_string] = required edition of the sequence for its matching to the genome ##ColumnVariable[chrom] = the name of the chromosome ##ColumnVariable[strand] = the strand in the chromosome ##ColumnVariable[start] = the starting position of the feature in the chromosome ##ColumnVariable[end] = the ending position of the feature in the chromosome ##ColumnVariable[percentage] = percent match (always 100) ##ColumnVariable[map_pos] = number of locations where this tag sequence mapped to the genome ##ColumnVariable[ribo_flag] = tag mapped to ribosome equal or better than chromosome? ##ColumnVariable[refseq_flag] = tag mapped to refseq better than chromosome? ##ColumnVariable[rna] = RNA name ##ColumnVariable[rna_count] = read count in the RNA ##ColumnVariable[tpm_in_ribo] = tag per million per timecourse including ribosome flagged tags ##ColumnVariable[tpm_ex_ribo] = tag per million per timecourse excluding ribosome_flagged tags ##ColumnVariable[weight] = weight of expression. This is just internal value, and please ignore this column for subsequent analysis ##ColumnVariable[rescue_weight] = weight from "guilt-by-association" rescue