Showing selected topics • reset
<prev • 44 results • page 1 of 2 • next >
0
votes
1
answer
86
views
1
answer
Pipes within VCF INFO Column
vcf exome-sequencing next-gen variant snp written 17 days ago by basay30 • updated 17 days ago by genomax80k
2
votes
0
answers
153
views
0
answers
BWA-MEM rather than bowtie2 in UKBB exome-sequencing alignment
exome-sequencing written 3 months ago by Shicheng Guo8.1k • updated 8 weeks ago by Biostar ♦♦ 20
0
votes
0
answers
207
views
0
answers
4
votes
0
answers
6.0k
views
0
answers
Hisat2 versus Bowtie2
bowtie2 exome-sequencing hisat2 written 3.9 years ago by nalpas.nicolas20 • updated 2.7 years ago by Biostar ♦♦ 20
6
votes
2
answers
1.3k
views
2
answers
Finding reads having more than one mutation in BAM file
R exome-sequencing next-gen bam written 3.6 years ago by marki60 • updated 3.6 years ago by WouterDeCoster43k
12
votes
3
answers
14k
views
7 follow
3
answers
14
votes
1
answer
5.2k
views
10 follow
1
answer
A Shift In Pca Plot For Population Stratification
exome-sequencing pca written 6.0 years ago by User 1933340 • updated 4.8 years ago by Zhenyu Zhang260
0
votes
0
answers
1.3k
views
0
answers
3
votes
2
answers
5.5k
views
2
answers
25
votes
6
answers
10k
views
20 follow
6
answers
1
vote
0
answers
1.9k
views
0
answers
1
vote
1
answer
2.7k
views
1
answer
5
votes
2
answers
5.3k
views
2
answers
Low Coverage Depth On Exome Sequencing
exome-sequencing coverage written 6.0 years ago by Nandini840 • updated 6.0 years ago by Katie D'Aco1000
1
vote
1
answer
3.0k
views
1
answer
Calculating Sequencing Depth Of A Genomic Region
vcf exome-sequencing written 6.0 years ago by User 1933340 • updated 6.0 years ago by Alex Paciorkowski3.4k
5
votes
1
answer
3.4k
views
1
answer
Help With The Dnacopy Number Package In R
exome-sequencing written 6.1 years ago by ivivek_ngs4.9k • updated 6.1 years ago by Sean Davis26k
15
votes
1
answer
3.2k
views
11 follow
1
answer
Music Analysis Workflow
exome-sequencing music snp cancer written 6.1 years ago by Pascal250 • updated 6.1 years ago by Cyriac Kandoth5.5k
1
vote
0
answers
2.1k
views
0
answers
Can We Call Variants Based On Alt Allele Frequncy?
gatk exome-sequencing annovar varscan written 6.1 years ago by ivivek_ngs4.9k • updated 6.1 years ago by Chris Miller21k
1
vote
2
answers
2.1k
views
2
answers
0
votes
0
answers
1.7k
views
0
answers
Rare Variants
exome-sequencing snps written 6.3 years ago by peris120 • updated 6.1 years ago by Biostar ♦♦ 20
2
votes
1
answer
3.3k
views
1
answer
1
vote
1
answer
3.0k
views
1
answer
Which To Consider As Non-Sense Mutation From Annovar Output?
annovar exome-sequencing gatk written 6.2 years ago by ivivek_ngs4.9k • updated 6.2 years ago by Ashutosh Pandey12k
0
votes
0
answers
1.0k
views
0
answers
1
vote
1
answer
3.3k
views
1
answer
1
vote
1
answer
1.6k
views
1
answer
1
vote
0
answers
2.9k
views
0
answers
1
vote
1
answer
7.3k
views
1
answer
Variant Filtration Using Gatk With Ad And Dp
gatk exome-sequencing written 6.3 years ago by ivivek_ngs4.9k • updated 6.3 years ago by Vivek2.4k
3
votes
2
answers
4.0k
views
5 follow
2
answers
Questions About Annotation Of Mouse Exome Variants Data By Annovar
mouse exome-sequencing annovar written 6.4 years ago by Tonyzeng300 • updated 6.3 years ago by Charles Warden7.6k
3
votes
1
answer
7.6k
views
1
answer
4
votes
1
answer
1.8k
views
1
answer
1
vote
4
answers
4.7k
views
5 follow
4
answers
<prev • 44 results • page 1 of 2 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1282 users visited in the last hour