SNPs call

[kurban910]

try this:

bcftools view my-raw.bcf| vcfutils.pl varFilter -d 10 > raw.vcf

then open raw.vcf in excel and you will see variants as snps or indels

(you might need to filter snps)

thank you, and i have found the tools i was looking for from here:

http://vcftools.sourceforge.net/man_latest.html

[mmmm]

try this:

bcftools view my-raw.bcf| vcfutils.pl varFilter -d 10 > raw.vcf

then open raw.vcf in excel and you will see variants as snps or indels

(you might need to filter snps)

[kurban910]

hello!
after a filtered my-raw.bcf file for SNPs i got the file my.var-final.bcf(27.1 MB). and when i open the file it opened ( by using gedit ), its content showed in this way:

##fileformat=VCFv4.1
##samtoolsVersion=0.1.18 (r982:295)
##INFO=<ID=DP,Number=1,Type=Integer,Description="Raw read depth">
##INFO=<ID=DP4,Number=4,Type=Integer,Description="# high-quality ref-forward bases, ref-reverse, alt-forward and alt-reverse bases">
##INFO=<ID=MQ,Number=1,Type=Integer,Description="Root-mean-square mapping quality of covering reads">
##INFO=<ID=FQ,Number=1,Type=Float,Description="Phred probability of all samples being the same">
##INFO=<ID=AF1,Number=1,Type=Float,Description="Max-likelihood estimate of the first ALT allele frequency (assuming HWE)">
##INFO=<ID=AC1,Number=1,Type=Float,Description="Max-likelihood estimate of the first ALT allele count (no HWE assumption)">
##INFO=<ID=G3,Number=3,Type=Float,Description="ML estimate of genotype frequencies">
##INFO=<ID=HWE,Number=1,Type=Float,Description="Chi^2 based HWE test P-value based on G3">
##INFO=<ID=CLR,Number=1,Type=Integer,Description="Log ratio of genotype likelihoods with and without the constraint">
##INFO=<ID=UGT,Number=1,Type=String,Description="The most probable unconstrained genotype configuration in the trio">
##INFO=<ID=CGT,Number=1,Type=String,Description="The most probable constrained genotype configuration in the trio">
##INFO=<ID=PV4,Number=4,Type=Float,Description="P-values for strand bias, baseQ bias, mapQ bias and tail distance bias">
##INFO=<ID=INDEL,Number=0,Type=Flag,Description="Indicates that the variant is an INDEL.">
##INFO=<ID=PC2,Number=2,Type=Integer,Description="Phred probability of the nonRef allele frequency in group1 samples being larger (,smaller) than in group2.">
##INFO=<ID=PCHI2,Number=1,Type=Float,Description="Posterior weighted chi^2 P-value for testing the association between group1 and group2 samples.">
##INFO=<ID=QCHI2,Number=1,Type=Integer,Description="Phred scaled PCHI2.">
##INFO=<ID=PR,Number=1,Type=Integer,Description="# permutations yielding a smaller PCHI2.">
##INFO=<ID=VDB,Number=1,Type=Float,Description="Variant Distance Bias">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=GL,Number=3,Type=Float,Description="Likelihoods for RR,RA,AA genotypes (R=ref,A=alt)">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="# high-quality bases">
##FORMAT=<ID=SP,Number=1,Type=Integer,Description="Phred-scaled strand bias P-value">
##FORMAT=<ID=PL,Number=G,Type=Integer,Description="List of Phred-scaled genotype likelihoods">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT my-sorted.bam
comp80_c0_seq1 12 . TAAAG T 10.8 . INDEL;DP=26;VDB=0.0000;AF1=0.5;AC1=1;DP4=19,0,4,0;MQ=60;FQ=13.7;PV4=1,1,1,0.49 GT:PL:GQ 0/1:48,0,255:50
comp904_c0_seq1 30 . G T 73.5 . DP=4;VDB=0.0014;AF1=1;AC1=2;DP4=0,0,4,0;MQ=60;FQ=-39 GT:PL:GQ 1/1:106,12,0:21
comp904_c0_seq1 37 . C T 52 . DP=4;VDB=0.0014;AF1=1;AC1=2;DP4=0,0,3,0;MQ=60;FQ=-36 GT:PL:GQ 1/1:84,9,0:16
comp904_c0_seq1 41 . A T 64.3 . DP=6;VDB=0.0020;AF1=1;AC1=2;DP4=0,0,5,0;MQ=60;FQ=-42 GT:PL:GQ

is there any way i can distinguish SNPs ( and indels if possible )form this file? if any how?

[mmmm]

if I have a file containing all SNPs- how to get some statistics such as snps differences among taxa, unique snps in certain taxa, etc. as it is taking forever to do this manually- is there a perl script please for this purpose

[BurlEarl]

Havn't used samtools for a pileup but many callers will filter out snps that are represented on only one strand. Is there a "failed snp" output you can compare?

[Brian Bushnell]

Can you post a screenshot of IGV? Also, make sure these reads have a high mapping quality and are not secondary alignments or multi-mapped.

[mmmm]

Hi all- when I am calling SNPs using samtools mpileup following mapping by BWA-

I get a list with the SNPs however, when I have a look at the bam file on IGV I can see other SNPs (that were not detected by samtools mpileup)- do you think what is the reason for this please?