* samtools-0.1.6-5 (r462)

[samtools.git] / samtools.1

diff --git a/samtools.1 b/samtools.1
index d2c78f1b32aeb00f4487f7944122ef9c7f5d596d..dee35abba1fb89c6dae1ec5cb3e5b83ebb92d0fe 100644 (file)
--- a/samtools.1
+++ b/samtools.1
@@ -220,14 +220,16 @@ mapping quality. A symbol `$' marks the end of a read segment.
 
 If option
 .B -c
-is applied, the consensus base, consensus quality, SNP quality and RMS
-mapping quality of the reads covering the site will be inserted between
-the `reference base' and the `read bases' columns. An indel occupies an
-additional line. Each indel line consists of chromosome name,
-coordinate, a star, the genotype, consensus quality, SNP quality, RMS
-mapping quality, # covering reads, the first alllele, the second allele,
-# reads supporting the first allele, # reads supporting the second
-allele and # reads containing indels different from the top two alleles.
+is applied, the consensus base, Phred-scaled consensus quality, SNP
+quality (i.e. the Phred-scaled probability of the consensus being
+identical to the reference) and root mean square (RMS) mapping quality
+of the reads covering the site will be inserted between the `reference
+base' and the `read bases' columns. An indel occupies an additional
+line. Each indel line consists of chromosome name, coordinate, a star,
+the genotype, consensus quality, SNP quality, RMS mapping quality, #
+covering reads, the first alllele, the second allele, # reads supporting
+the first allele, # reads supporting the second allele and # reads
+containing indels different from the top two alleles.
 
 .B OPTIONS:
 .RS
@@ -322,8 +324,6 @@ Text alignment viewer (based on the ncurses library). In the viewer,
 press `?' for help and press `g' to check the alignment start from a
 region in the format like `chr10:10,000,000'.
 
-.RE
-
 .TP
 .B fixmate
 samtools fixmate <in.nameSrt.bam> <out.bam>
@@ -341,8 +341,6 @@ This command
 .B ONLY
 works with FR orientation and requires ISIZE is correctly set.
 
-.RE
-
 .TP
 .B rmdupse
 samtools rmdupse <input.srt.bam> <out.bam>
@@ -350,8 +348,6 @@ samtools rmdupse <input.srt.bam> <out.bam>
 Remove potential duplicates for single-ended reads. This command will
 treat all reads as single-ended even if they are paired in fact.
 
-.RE
-
 .TP
 .B fillmd
 samtools fillmd [-e] <aln.bam> <ref.fasta>