Showing selected topics • reset
<prev • 12 results • page 1 of 1 • next >
5
votes
2
answers
3.0k
views
2
answers
Copy Number Variation Steps (CNVs) - detection step by step
genome ngs sequence snp cnvs written 3.9 years ago by elsayedhegazy20 • updated 3.9 years ago by Medhat8.7k
6
votes
0
answers
2.0k
views
5 follow
0
answers
0
votes
2
answers
1.0k
views
2
answers
Detection of CNVs
gatk cnvs written 3.7 years ago by nkausthu20 • updated 3.7 years ago by chen2.0k
1
vote
1
answer
960
views
1
answer
0
votes
1
answer
858
views
1
answer
Merge CNVnator and Lumpy to find out copy number variants
svs cnvs written 17 months ago by Mbillah110 • updated 12 months ago by Mant0
0
votes
0
answers
776
views
0
answers
panelcn.MOPS description of methodology
cnvs written 3.1 years ago by agata88790
3
votes
1
answer
739
views
1
answer
best way to separate copy number variations from VCF files
snp cnvs written 19 months ago by soleimani_homa0 • updated 19 months ago by WouterDeCoster43k
1
vote
2
answers
307
views
2
answers
0
votes
0
answers
162
views
0
answers
2
votes
0
answers
140
views
0
answers
Call CNVs using gene positions
read depth cnvs sequencing written 4 months ago by shinken12390 • updated 3 months ago by Biostar ♦♦ 20
0
votes
1
answer
125
views
1
answer
Calling CNVs in exomes - CLAMMS
exome next-gen clamms cnvs sequencing written 3 months ago by kath.a.fawcett0 • updated 6 days ago by lakhujanivijay5.0k
0
votes
0
answers
51
views
0
answers
CNV calling on WGS only on gene positions
cnvkit cnvcalling cnvs written 10 days ago by pabloatienzalo0 • updated 10 days ago by RamRS27k
<prev • 12 results • page 1 of 1 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1493 users visited in the last hour