X-Git-Url: https://git.donarmstrong.com/?a=blobdiff_plain;f=samtools.1;h=5923abd52608ee9003cbe17c49e93755f67a647f;hb=8e3b3f229a04cb81b680987ce06ae1507c9d8b69;hp=4b3f75a1926f0c4248f228f6378d2ff06e3e0c77;hpb=125ac895854cf760a04192a257a4279f2c541164;p=samtools.git diff --git a/samtools.1 b/samtools.1 index 4b3f75a..5923abd 100644 --- a/samtools.1 +++ b/samtools.1 @@ -1,4 +1,4 @@ -.TH samtools 1 "2 September 2011" "samtools-0.1.18" "Bioinformatics tools" +.TH samtools 1 "15 March 2013" "samtools-0.1.19" "Bioinformatics tools" .SH NAME .PP samtools - Utilities for the Sequence Alignment/Map (SAM) format @@ -353,7 +353,7 @@ which enables fast BAM concatenation. .TP .B sort -samtools sort [-no] [-m maxMem] +samtools sort [-nof] [-m maxMem] Sort alignments by leftmost coordinates. File .I .bam @@ -371,6 +371,13 @@ Output the final alignment to the standard output. .B -n Sort by read names rather than by chromosomal coordinates .TP +.B -f +Use +.I +as the full output path and do not append +.I .bam +suffix. +.TP .BI -m \ INT Approximately the maximum required memory. [500000000] .RE @@ -974,6 +981,25 @@ tag set to Collecting indel candidates from reads sequenced by an indel-prone technology may affect the performance of indel calling. +Note that there is a new calling model which can be invoked by + + bcftools view -m0.99 ... + +which fixes some severe limitations of the default method. + +For filtering, best results seem to be achieved by first applying the +.IR SnpGap +filter and then applying some machine learning approach + + vcf-annotate -f SnpGap=n + vcf filter ... + +Both can be found in the +.B vcftools +and +.B htslib +package (links below). + .IP o 2 Derive the allele frequency spectrum (AFS) on a list of sites from multiple individuals: @@ -1032,3 +1058,9 @@ specification. .SH SEE ALSO .PP Samtools website: +.br +Samtools latest source: +.br +VCFtools website with stable link to VCF specification: +.br +HTSlib website: