Showing: wgsreset
<prev • 246 results • page 1 of 9 • next >
7
votes
1
answer
110
views
1
answer
1
vote
0
answers
972
views
0
answers
1
vote
1
answer
116
views
1
answer
2
votes
0
answers
234
views
6 follow
0
answers
Extract sequences from the raw reads
wgs next-gen written 10 weeks ago by Jusnib0 • updated 5 weeks ago by Biostar ♦♦ 20
1
vote
0
answers
195
views
0
answers
Finding/Generating Example WGS Data With Transgene
transgene wgs insert data example written 11 weeks ago by sallehl0 • updated 5 weeks ago by Biostar ♦♦ 20
0
votes
1
answer
164
views
1
answer
3
votes
1
answer
154
views
1
answer
0
votes
0
answers
153
views
0
answers
7
votes
1
answer
208
views
1
answer
Only females but still few reads map to Y chromosome
wgs alignment bwa written 9 weeks ago by serpalma.v20 • updated 9 weeks ago by Pierre Lindenbaum116k
1
vote
0
answers
108
views
0
answers
0
votes
0
answers
152
views
0
answers
0
votes
1
answer
206
views
1
answer
Calling CNVs from WGS data
sv wgs sequencing cnv bioinformatics written 3 months ago by CH0 • updated 3 months ago by Chris Miller20k
0
votes
0
answers
305
views
0
answers
Problem with WGS
assembly wgs written 5 months ago by aggsandy80 • updated 3 months ago by Biostar ♦♦ 20
4
votes
2
answers
185
views
2
answers
Count 0, 5, 20 covered sites in bam
wgs bam written 3 months ago by DVA480 • updated 3 months ago by Pierre Lindenbaum116k
0
votes
0
answers
163
views
0
answers
Pangenome from bam files
sequence wgs pangenome bam written 3 months ago by ssj2620
13
votes
1
answer
265
views
5 follow
1
answer
Paternity Testing from WGS Trio
trio wgs dna-seq paternity test written 4 months ago by ClkElf20 • updated 4 months ago by RamRS20k
1
vote
1
answer
297
views
1
answer
bcftools: DP filter based on chromosome and sex
wgs pyvcf bcftools samtools vcftools written 4 months ago by bsmith030465120 • updated 4 months ago by Pierre Lindenbaum116k
1
vote
1
answer
198
views
1
answer
Human CNV VCF for Trios from whole-genomes
wgs cnv trios written 4 months ago by hellbio340 • updated 4 months ago by trausch1.2k
2
votes
1
answer
281
views
1
answer
faster variant annotation for large VCFs
vcf wgs variant annotation written 4 months ago by Amitm1.6k • updated 4 months ago by Emily_Ensembl16k
1
vote
2
answers
227
views
2
answers
what is the conventional apporach to calculate depth of coverage?
wgs dnaseq coverage snp depth written 4 months ago by serpalma.v20 • updated 4 months ago by finswimmer8.8k
1
vote
2
answers
203
views
2
answers
0
votes
0
answers
258
views
0
answers
1
vote
1
answer
235
views
1
answer
download WGS from dbGAP authorized with prefetch tools
wgs dbgap written 4 months ago by jonessara770130 • updated 4 months ago by ATpoint12k
1
vote
0
answers
228
views
0
answers
1
vote
1
answer
172
views
1
answer
Mycobacterium whole genome sequencing
wgs ngs mycobacterium written 5 months ago by drparomita.bhatt0 • updated 5 months ago by Vijay Lakhujani3.5k
1
vote
0
answers
193
views
0
answers
0
votes
0
answers
395
views
0
answers
0
votes
0
answers
215
views
0
answers
0
votes
0
answers
194
views
0
answers
using the docker container of cgpPINDEL
indel wgs snv pindel written 7 months ago by Bogdan690 • updated 5 months ago by Biostar ♦♦ 20
0
votes
0
answers
255
views
0
answers
<prev • 246 results • page 1 of 9 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1192 users visited in the last hour