Showing: snpreset
<prev • 4,297 results • page 1 of 144 • next >
2
votes
0
answers
122
views
0
answers
Losing somatic SNPs
varscan snp varaft written 28 days ago by gab0 • updated 3 hours ago by Biostar ♦♦ 20
1
vote
1
answer
81
views
1
answer
SNPs genomic classification based on VCF annotation
R snp written 7 hours ago by aarvaBioinfo10 • updated 4 hours ago by finswimmer4.5k
0
votes
0
answers
78
views
0
answers
maftools - no chromosomal coordinates
R bioconductor snp written 16 hours ago by sumithrasank7590 • updated 13 hours ago by zx87544.8k
0
votes
0
answers
84
views
0
answers
how to detect mutation from viral RNA-seq data
R rna-seq snp sequencing written 15 hours ago by babasaraki0 • updated 14 hours ago by grant.hovhannisyan1.0k
10
votes
0
answers
231
views
6 follow
0
answers
6
votes
1
answer
92
views
1
answer
Extract SNPs from VCFfile located in genes based on GFF file information
gene snp written 18 hours ago by Denis30 • updated 17 hours ago by finswimmer4.5k
2
votes
3
answers
194
views
3
answers
Kissplice: Problem getting SNPs in test data
snp kissplice written 4 months ago by WeepingMeadow0 • updated 19 hours ago by leandro.ishi.lima80
2
votes
1
answer
60
views
1
answer
Subset analyze of multiple sample file in PLINK 1.9
sequence plink snp written 1 day ago by mike229lin10 • updated 20 hours ago by zx87544.8k
0
votes
0
answers
46
views
0
answers
0
votes
1
answer
108
views
1
answer
0
votes
1
answer
704
views
1
answer
Nan in expectationUNR
software error gene snp genome written 23 months ago by yxwang60 • updated 1 day ago by emamy2020
8
votes
3
answers
2.2k
views
7 follow
3
answers
how can i remove duplicated variants from vcf file?
vcf snp written 13 months ago by kk.mahsa70 • updated 3 days ago by Shicheng Guo6.1k
2
votes
0
answers
117
views
0
answers
0
votes
0
answers
68
views
0
answers
Extract a list of SNPs from a BCF file
bcf snp written 3 days ago by Fersal0 • updated 3 days ago by genomax54k
1
vote
0
answers
778
views
0
answers
Use PacBio's iso-seq data to look for variant
next-gen snp sequencing written 2.2 years ago by yanweng30 • updated 4 days ago by Biostar ♦♦ 20
2
votes
1
answer
12k
views
1
answer
Bcftools view options for SNPs calling.
bcftools samtools snp mpileup written 3.1 years ago by Eddie_I10 • updated 4 days ago by Kevin Blighe26k
2
votes
1
answer
132
views
1
answer
Variant Allele Frequency
vcf samtools snp written 5 days ago by kspata30 • updated 4 days ago by btsui230
0
votes
0
answers
104
views
0
answers
what value reflect the admixture dates in the logfile Using ALDER
alder admixture time snp written 10 weeks ago by zhangmingpeng0 • updated 4 days ago by Biostar ♦♦ 20
1
vote
1
answer
130
views
1
answer
How calculate MAF from impute2 output in R
maf impute2 snp written 7 weeks ago by vgenepi10 • updated 4 days ago by zx87544.8k
1
vote
1
answer
98
views
1
answer
1
vote
1
answer
118
views
5 follow
1
answer
0
votes
0
answers
70
views
0
answers
0
votes
1
answer
82
views
1
answer
0
votes
0
answers
107
views
0
answers
Short Variants calling error when using bcftools mpileup
genome alignment snp written 6 days ago by mike229lin10 • updated 6 days ago by finswimmer4.5k
0
votes
0
answers
77
views
0
answers
3
votes
1
answer
105
views
1
answer
6
votes
1
answer
129
views
1
answer
What is the difference between HaplotypeCaller and UnifiedGenotyper?
snp written 7 days ago by mostafarafiepour0 • updated 7 days ago by finswimmer4.5k
1
vote
1
answer
106
views
1
answer
Updating INDEL SNP positions
snp written 7 days ago by drakejh0 • updated 7 days ago by finswimmer4.5k
6
votes
2
answers
725
views
2
answers
RNA-seq experimental design for SNP calling
rna-seq snp written 12 months ago by windhavenn20 • updated 8 days ago by andrew.j.skelton735.2k
0
votes
0
answers
97
views
0
answers
<prev • 4,297 results • page 1 of 144 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1739 users visited in the last hour