<prev • 64,813 results • page 1 of 2161 • next >
0
votes
0
answers
5
views
0
answers
4
votes
2
answers
12
views
2
answers
How do I get the strand of a read when using htslib?
htslib written 18 minutes ago by Click downvote620 • updated 3 minutes ago by Alex Reynolds26k
0
votes
0
answers
11
views
0
answers
2
votes
1
answer
28
views
1
answer
how to set metrics file when using MarkDuplicates in Picard
software error genome picard written 1 hour ago by Yingzi Zhang30 • updated 46 minutes ago by zx87545.3k
0
votes
1
answer
29
views
1
answer
How to separate a strain of MTB drug wise?
python grep sed loop awk written 3 hours ago by angelshiza10 • updated 22 minutes ago by rizoic50
0
votes
0
answers
30
views
0
answers
0
votes
0
answers
39
views
0
answers
0
votes
1
answer
53
views
1
answer
ANNOVAR annotate frameshift
annovar mutation variant exonic written 8 hours ago by sugus20 • updated 7 hours ago by Kevin Blighe30k
0
votes
0
answers
51
views
0
answers
1
vote
0
answers
71
views
0
answers
0
votes
0
answers
73
views
0
answers
Separate Genome into Tiers
genome written 11 hours ago by angrypigeon120
1
vote
0
answers
72
views
5 follow
0
answers
To fetch the reads which are being partially mapped to the genome
jvarkit hisat2 star rna-seq bowtie2 written 11 hours ago by swadha20 • updated 10 hours ago by genomax57k
0
votes
0
answers
93
views
0
answers
0
votes
1
answer
65
views
1
answer
GC content analysis using EdgeR
rna-seq written 13 hours ago by vhelizarraga0 • updated 13 hours ago by h.mon20k
0
votes
0
answers
50
views
0
answers
0
votes
1
answer
63
views
1
answer
Diploid sequences in ModelTest-NG: consensus or ambiguous sites?
next-gen diploid modeltest written 15 hours ago by CaffeSospeso0 • updated 13 hours ago by Vitis1.6k
0
votes
1
answer
82
views
1
answer
Infer direction of paired end data
rna-seq written 16 hours ago by waqaskhokhar9990 • updated 16 hours ago by Istvan Albert ♦♦ 77k
2
votes
1
answer
96
views
1
answer
0
votes
1
answer
59
views
1
answer
cell type specific TAD coordinates and orientations for Hi-C
sequencing written 17 hours ago by alireza3460 • updated 17 hours ago by jared.andrews071.3k
0
votes
0
answers
69
views
0
answers
2
votes
0
answers
102
views
5 follow
0
answers
0
votes
1
answer
103
views
1
answer
Is TCGA Breast cancer data strand specific?
geneexpression tcga rna-seq strand hisat2 written 19 hours ago by Bioinfo270 • updated 18 hours ago by genomax57k
2
votes
0
answers
78
views
0
answers
1
vote
0
answers
56
views
0
answers
19
votes
4
answers
284
views
9 follow
4
answers
manipulating a file by R or bash?
text parsing R bash written 20 hours ago by Za120 • updated 9 hours ago by Chirag Parsania1.1k
0
votes
0
answers
73
views
0
answers
0
votes
0
answers
63
views
0
answers
Extracting Flanking Regions using Biopython
bedtools biopython written 21 hours ago by LindoNkambule0 • updated 21 hours ago by jrj.healey7.6k
1
vote
2
answers
95
views
2
answers
Time-course RNA-seq analysis in Deseq2
R rna-seq written 21 hours ago by Lisa300 • updated 13 hours ago by Vitis1.6k
0
votes
0
answers
46
views
0
answers
Rare variants imputation
imputation sequencing written 22 hours ago by reds.nik30
2
votes
0
answers
95
views
0
answers
Python Script to Calculate Total Number of genes
python script hapatatis c virus written 22 hours ago by anasjamshed19940 • updated 22 hours ago by finswimmer6.2k
<prev • 64,813 results • page 1 of 2161 • next >

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 1921 users visited in the last hour