Showing selected topics • reset
<prev • 6,884 results • page 1 of 230 • next >
1
vote
0
answers
28
views
0
answers
Regarding Barley genome
gene assembly genome written 3 hours ago by umeshtanwar220
0
votes
1
answer
31
views
1
answer
Calculating minor allele frequency for GnomAD VCF file
genome gnomad written 6 hours ago by Jamie Watson0 • updated 4 hours ago by Jeremy Leipzig19k
3
votes
1
answer
72
views
1
answer
0
votes
0
answers
31
views
0
answers
0
votes
0
answers
63
views
0
answers
Why might a large number of variants fail HWE?
genome rna-seq snp written 6 days ago by srmeetd0 • updated 9 hours ago by i.sudbery9.7k
2
votes
1
answer
88
views
1
answer
How to get the sequence differences between multiple bacterial genomes
genome alignment written 14 hours ago by Rose0 • updated 11 hours ago by shenwei3565.6k
1
vote
0
answers
27
views
0
answers
2
votes
1
answer
49
views
1
answer
genome coverage visualization
genome bedtools bam coverage written 1 day ago by gabri.mochales40 • updated 19 hours ago by bernatgel2.7k
0
votes
0
answers
25
views
0
answers
5
votes
2
answers
111
views
2
answers
0
votes
0
answers
29
views
0
answers
0
votes
1
answer
51
views
1
answer
0
votes
0
answers
44
views
0
answers
how to get input file of closest-features a bed-format file
genome gene sequencing written 2 days ago by MEITUO10 • updated 2 days ago by jordi.planells270
0
votes
0
answers
57
views
0
answers
0
votes
0
answers
197
views
0
answers
0
votes
0
answers
51
views
0
answers
1
vote
1
answer
65
views
1
answer
Converting tsv into bam file
genome R sequencing linux written 4 days ago by vinayjrao180 • updated 4 days ago by swbarnes29.1k
19
votes
4
answers
198
views
10 follow
4
answers
Forum: DNA in pixels
genome forum alignment sequencing written 7 days ago by mervsen30 • updated 4 days ago by cmarmanjuriya0
0
votes
0
answers
52
views
0
answers
Haplotyping Using Whatshap
genome sequence alignment snp written 4 days ago by wangyunyang0 • updated 4 days ago by h.mon31k
0
votes
0
answers
46
views
0
answers
1
vote
1
answer
381
views
1
answer
P-hacking or not in pan-cancer analysis
p-value genome pan-cancer written 2.0 years ago by Wenhu_Cao70 • updated 5 days ago by Jean-Karim Heriche23k
1
vote
0
answers
111
views
0
answers
Extracting CDS using python
genome python gbk written 5 days ago by Davi.marcon0 • updated 5 days ago by h.mon31k
1
vote
1
answer
359
views
1
answer
How to obtain sequences of long insertion in VCF of 1000 genome project
genome written 11 months ago by ks0 • updated 6 days ago by vincenzo.bonnici0
1
vote
1
answer
1.3k
views
1
answer
reference genome for 16S rDNA sequences in NGS analysis
ref next-gen 16s alignment genome written 4.7 years ago by Ybanet0 • updated 6 days ago by jazebe_14610
0
votes
0
answers
239
views
0
answers
0
votes
0
answers
46
views
0
answers
0
votes
1
answer
59
views
1
answer
bedtools intersect and find genes
genome written 6 days ago by hosein_salehi60 • updated 6 days ago by ATpoint41k
6
votes
2
answers
96
views
5 follow
2
answers
1
vote
3
answers
86
views
3
answers
bedtools sort and merge
genome written 8 days ago by hosein_salehi60 • updated 8 days ago by Alex Reynolds31k
3
votes
1
answer
63
views
1
answer
<prev • 6,884 results • page 1 of 230 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1657 users visited in the last hour