Showing: variant callingreset
<prev • 152 results • page 1 of 6 • next >
0
votes
3
answers
86
views
6 follow
3
answers
0
votes
0
answers
104
views
0
answers
4
votes
2
answers
656
views
2
answers
1
vote
1
answer
125
views
1
answer
3
votes
0
answers
245
views
0
answers
Base Recabiliration Filters out 88% of the reads
variant calling rna-seq written 10 weeks ago by Sharon250 • updated 14 days ago by Biostar ♦♦ 20
3
votes
0
answers
123
views
0
answers
5
votes
2
answers
90
views
6 follow
2
answers
Variant calling in genomic chunks
variant calling vcf written 15 days ago by Damian Kao14k • updated 14 days ago by finswimmer1.5k
11
votes
5
answers
244
views
8 follow
5
answers
3
votes
1
answer
188
views
1
answer
Should we discard a variant if it pass many filters and fails one?
variant calling written 4 weeks ago by Sharon250 • updated 23 days ago by Biostar ♦♦ 20
3
votes
1
answer
123
views
1
answer
4
votes
2
answers
167
views
5 follow
2
answers
Somatic vs Germline Variant Calling
variant calling somatic sequencing germline written 4 weeks ago by checkyodna0 • updated 4 weeks ago by Ram14k
5
votes
1
answer
1.4k
views
1
answer
How to visualize large VCF files
vcf variant calling snps variant snp written 23 months ago by bioinforesearchquestions120 • updated 4 weeks ago by Biostar ♦♦ 20
2
votes
0
answers
148
views
0
answers
0
votes
1
answer
224
views
1
answer
Bedtools intersect error
bedtools vcf .bed variant calling gatk written 5 weeks ago by jaqx00810 • updated 5 weeks ago by Alex Reynolds23k
0
votes
2
answers
244
views
2
answers
5
votes
0
answers
102
views
5 follow
0
answers
2
votes
1
answer
87
views
1
answer
Why FS is low when reads aligned from strand seem biased?
exome variant calling vcf written 5 weeks ago by Sharon250 • updated 5 weeks ago by finswimmer1.5k
4
votes
1
answer
218
views
1
answer
Having Issues with Variant Calling
variant calling samtools snp sequencing written 6 weeks ago by shola_aleru10 • updated 6 weeks ago by Pierre Lindenbaum106k
0
votes
1
answer
102
views
1
answer
9
votes
2
answers
188
views
5 follow
2
answers
6
votes
1
answer
156
views
1
answer
How many reads needed to be sure a variant does not exist?
variant calling written 7 weeks ago by steve1.4k • updated 7 weeks ago by Gabriel R.2.4k
0
votes
1
answer
209
views
1
answer
Basics about sequencing/alignment and variant calling
variant calling alignment sequencing written 8 weeks ago by ernestrv01010 • updated 7 weeks ago by d-cameron1.5k
7
votes
3
answers
1.2k
views
3
answers
Multisample vcf to table
variant calling snp sequencing written 22 months ago by Myggan20 • updated 8 weeks ago by kirannbishwa01780
1
vote
0
answers
151
views
0
answers
0
votes
0
answers
132
views
0
answers
0
votes
0
answers
128
views
0
answers
2
votes
1
answer
192
views
1
answer
Understanding the VCF data from my variant calling
vcf variant calling snps igv indels written 9 weeks ago by jaqx00810 • updated 9 weeks ago by jared.andrews07680
0
votes
1
answer
269
views
1
answer
hg19 or hg38 for variant calling
genome variant calling assembly written 9 weeks ago by jsneaththompson40 • updated 9 weeks ago by h.mon13k
1
vote
1
answer
217
views
1
answer
2
votes
0
answers
285
views
0
answers
<prev • 152 results • page 1 of 6 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1109 users visited in the last hour