/* * The MIT License * * Copyright (c) 2011 The Broad Institute * * Permission is hereby granted, free of charge, to any person obtaining a copy * of this software and associated documentation files (the "Software"), to deal * in the Software without restriction, including without limitation the rights * to use, copy, modify, merge, publish, distribute, sublicense, and/or sell * copies of the Software, and to permit persons to whom the Software is * furnished to do so, subject to the following conditions: * * The above copyright notice and this permission notice shall be included in * all copies or substantial portions of the Software. * * THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR * IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY, * FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE * AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER * LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM, * OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN * THE SOFTWARE. */ package picard.analysis; import picard.metrics.MultilevelMetrics; /** * Metrics about the alignment of RNA-seq reads within a SAM file to genes, produced by the CollectRnaSeqMetrics * program and usually stored in a file with the extension ".rna_metrics". */ public class RnaSeqMetrics extends MultilevelMetrics { /** The total number of PF bases including non-aligned reads. */ public long PF_BASES; /** * The total number of aligned PF bases. Non-primary alignments are not counted. Bases in aligned reads that * do not correspond to reference (e.g. soft clips, insertions) are not counted. */ public long PF_ALIGNED_BASES; /** Number of bases in primary aligments that align to ribosomal sequence. */ public Long RIBOSOMAL_BASES; /** Number of bases in primary aligments that align to a non-UTR coding base for some gene, and not ribosomal sequence. */ public long CODING_BASES; /** Number of bases in primary aligments that align to a UTR base for some gene, and not a coding base. */ public long UTR_BASES; /** Number of bases in primary aligments that align to an intronic base for some gene, and not a coding or UTR base. */ public long INTRONIC_BASES; /** Number of bases in primary aligments that do not align to any gene. */ public long INTERGENIC_BASES; /** * Number of primary alignments that map to a sequence specified on command-line as IGNORED_SEQUENCE. These are not * counted in PF_ALIGNED_BASES, CORRECT_STRAND_READS, INCORRECT_STRAND_READS, or any of the base-counting metrics. * These reads are counted in PF_BASES. */ public long IGNORED_READS; /** Number of aligned reads that map to the correct strand. 0 if library is not strand-specific. */ public long CORRECT_STRAND_READS; /** Number of aligned reads that map to the incorrect strand. 0 if library is not strand-specific. */ public long INCORRECT_STRAND_READS; /** RIBOSOMAL_BASES / PF_ALIGNED_BASES */ public Double PCT_RIBOSOMAL_BASES; /** CODING_BASES / PF_ALIGNED_BASES */ public double PCT_CODING_BASES; /** UTR_BASES / PF_ALIGNED_BASES */ public double PCT_UTR_BASES; /** INTRONIC_BASES / PF_ALIGNED_BASES */ public double PCT_INTRONIC_BASES; /** INTERGENIC_BASES / PF_ALIGNED_BASES */ public double PCT_INTERGENIC_BASES; /** PCT_UTR_BASES + PCT_CODING_BASES */ public double PCT_MRNA_BASES; /** The percentage of bases mapping to mRNA divided by the total number of PF bases. */ public double PCT_USABLE_BASES; /** CORRECT_STRAND_READS/(CORRECT_STRAND_READS + INCORRECT_STRAND_READS). 0 if library is not strand-specific. */ public double PCT_CORRECT_STRAND_READS; /** The median CV of coverage of the 1000 most highly expressed transcripts. Ideal value = 0. */ public double MEDIAN_CV_COVERAGE; /** * The median 5 prime bias of the 1000 most highly expressed transcripts, where 5 prime bias is calculated per * transcript as: mean coverage of the 5' most 100 bases divided by the mean coverage of the whole transcript. */ public double MEDIAN_5PRIME_BIAS; /** * The median 3 prime bias of the 1000 most highly expressed transcripts, where 3 prime bias is calculated per * transcript as: mean coverage of the 3' most 100 bases divided by the mean coverage of the whole transcript. */ public double MEDIAN_3PRIME_BIAS; /** The ratio of coverage at the 5' end of to the 3' end based on the 1000 most highly expressed transcripts. */ public double MEDIAN_5PRIME_TO_3PRIME_BIAS; }