Showing: variant callingreset
<prev • 119 results • page 1 of 4 • next >
2
votes
2
answers
137
views
2
answers
Infer somatic mutations without normal control
variant calling somatic mutation written 9 days ago by CY80 • updated 6 days ago by markus.riester230
0
votes
0
answers
192
views
0
answers
0
votes
0
answers
81
views
0
answers
0
votes
1
answer
103
views
1
answer
GATK Variant calling
variant calling gatk snps written 8 days ago by jaqx0080 • updated 8 days ago by finswimmer660
0
votes
1
answer
141
views
1
answer
Error in Generating sorted.bam
variant calling gatk .sam rna-seq written 5 weeks ago by jaqx0080 • updated 5 weeks ago by genomax40k
12
votes
5
answers
1.8k
views
6 follow
5
answers
1
vote
0
answers
161
views
0
answers
0
votes
1
answer
157
views
1
answer
1
vote
0
answers
193
views
0
answers
2
votes
1
answer
148
views
1
answer
some good practices doubts
gene variant calling alignment written 9 weeks ago by prasundutta87150 • updated 9 weeks ago by WouterDeCoster24k
3
votes
1
answer
374
views
1
answer
18
votes
7
answers
1.2k
views
7
answers
3
votes
0
answers
165
views
0
answers
18
votes
3
answers
1.3k
views
3
answers
0
votes
1
answer
320
views
1
answer
bwa mem: Passing a variable to read group
variant calling bwa-mem alignment bwa gatk written 11 weeks ago by rmf100 • updated 11 weeks ago by Pierre Lindenbaum103k
2
votes
1
answer
169
views
1
answer
Identify homopolymer stretches in a given genome
variant calling indel homopolymers snp written 11 weeks ago by ATPoint2.6k • updated 11 weeks ago by Pierre Lindenbaum103k
3
votes
3
answers
384
views
3
answers
How to make variant calling run faster?
variant calling gatk mutect2 written 3 months ago by steve1.3k • updated 3 months ago by Brian Bushnell15k
10
votes
3
answers
460
views
6 follow
3
answers
DNA sequence of genes from vcf file
vcf variant calling bcftools gene ensembl written 5 months ago by bioinfo890 • updated 3 months ago by songbaoxing1680
3
votes
0
answers
221
views
0
answers
Detecting gene insertions with DiscoSNP
variant calling discosnp written 4 months ago by laeb60 • updated 3 months ago by Biostar ♦♦ 20
2
votes
1
answer
294
views
1
answer
What does ALT 0 mean in a VCF?
variant calling sequence alignment written 4 months ago by emyli0 • updated 4 months ago by finswimmer660
1
vote
1
answer
254
views
1
answer
0
votes
0
answers
175
views
0
answers
0
votes
0
answers
190
views
0
answers
1
vote
1
answer
367
views
1
answer
HaplotypeCaller filter out variants covered only in one direction
variant calling gatk haplotype caller written 4 months ago by stanedav10 • updated 4 months ago by pfs200
2
votes
1
answer
288
views
1
answer
2
votes
2
answers
324
views
2
answers
2
votes
0
answers
253
views
0
answers
Retain file names as sample names while making pileup
vcf variant calling bcftools samtools gene written 5 months ago by bioinfo890 • updated 5 months ago by WouterDeCoster24k
6
votes
1
answer
463
views
1
answer
snpEff inappropriate interpretation of variants?
software error variant calling alignment rna-seq written 5 months ago by moushengxu290 • updated 5 months ago by rbagnall1.1k
9
votes
3
answers
357
views
7 follow
3
answers
6
votes
2
answers
360
views
2
answers
how to calling variants in RNAseq data from multiple samples?
variant calling gatk vc rna-seq written 6 months ago by Lila M 370 • updated 6 months ago by Samuel Brady230
<prev • 119 results • page 1 of 4 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 830 users visited in the last hour