Showing: varscanreset
<prev • 75 results • page 1 of 3 • next >
0
votes
0
answers
94
views
0
answers
0
votes
1
answer
562
views
1
answer
varscan v2.3.9 filter Parse exception
varscan written 12 months ago by cafelumiere1270 • updated 24 days ago by jlx02480
1
vote
1
answer
206
views
1
answer
How to exclude noisy CNV from study?
dnacopy varscan copy number variation cnv wes written 10 weeks ago by rmateos.110 • updated 6 weeks ago by vchris_ngs3.1k
1
vote
2
answers
1.8k
views
2
answers
Problems After Loading Varscan 2 Output Into Bioconductor.Dnacopy
exome varscan copynumber cnv sequencing written 4.2 years ago by sousuffer20 • updated 6 weeks ago by Biostar ♦♦ 20
0
votes
0
answers
208
views
0
answers
0
votes
0
answers
104
views
0
answers
0
votes
0
answers
173
views
0
answers
1
vote
0
answers
511
views
0
answers
varscan2 mpileup2snp output contains indels
vcf indels mpileup2snp varscan written 14 months ago by AW280 • updated 3 months ago by Biostar ♦♦ 20
2
votes
0
answers
317
views
0
answers
What allele frequency threshold do you recommend?
varscan written 5 months ago by agata88540 • updated 3 months ago by Biostar ♦♦ 20
1
vote
0
answers
249
views
0
answers
0
votes
1
answer
262
views
1
answer
0
votes
0
answers
196
views
0
answers
0
votes
0
answers
348
views
0
answers
4
votes
0
answers
469
views
0
answers
Exome-seq; Which tools to predict significantly muated genes .
varscan music cnv written 7 months ago by Chirag Nepal1.8k • updated 6 months ago by Biostar ♦♦ 20
4
votes
1
answer
392
views
1
answer
Gold Standard for Human cancer exome sequencing
somatic wes varscan mutect cancer written 6 months ago by Jerome Lin10 • updated 6 months ago by harold.smith.tarheel3.5k
0
votes
0
answers
174
views
0
answers
Varscan mpileup2snp coverage filter
mpileup2snp varscan written 6 months ago by AW280
0
votes
0
answers
274
views
0
answers
11
votes
1
answer
386
views
1
answer
Variant Calling in Somatic mode
vcf varscan variants snp sequencing written 7 months ago by Paul530 • updated 7 months ago by venu3.7k
0
votes
1
answer
480
views
1
answer
sciClone:input data wrong
dnacopy varscan copy number sciclone cluster written 7 months ago by lyan.liu0 • updated 7 months ago by Chris Miller18k
0
votes
1
answer
499
views
1
answer
indel preprocessing prior to bam-readcount
indel varscan fpfilter.pl bam-readcount written 8 months ago by Jokhe40 • updated 7 months ago by m.b0
0
votes
2
answers
665
views
2
answers
Finding SNPs per gene for SNP Density in UNIX
varscan grep unix snp written 18 months ago by crawlthrutacos0 • updated 9 months ago by Alex Reynolds19k
0
votes
0
answers
356
views
0
answers
2
votes
1
answer
815
views
1
answer
VarScan and Samtools - how to process my data?
varscan ngs sequencing samtools pipeline written 10 months ago by aagata.szymanek10 • updated 10 months ago by poisonAlien2.2k
2
votes
0
answers
472
views
0
answers
0
votes
0
answers
438
views
0
answers
10
votes
2
answers
875
views
2
answers
0
votes
0
answers
388
views
0
answers
2
votes
1
answer
1.1k
views
1
answer
2
votes
1
answer
1.1k
views
1
answer
6
votes
2
answers
2.0k
views
2
answers
Varscan Somatic...Syntax To Run With Redirect?
varscan samtools written 6.0 years ago by Hmm490 • updated 21 months ago by Biostar ♦♦ 20
<prev • 75 results • page 1 of 3 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 940 users visited in the last hour