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354
votes
16
answers
24k
views
164 follow
16
answers
News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 18 months ago by Istvan Albert ♦♦ 77k • updated 13 hours ago by Vijay Lakhujani2.5k
16
votes
4
answers
2.7k
views
8 follow
4
answers
Has Anyone Tried Rum For Aligning/Counting Illumina Rna-Seq Data?
alignment rna written 6.9 years ago by Travis2.8k • updated 3 hours ago by Biostar ♦♦ 20
5
votes
1
answer
2.4k
views
1
answer
2
votes
1
answer
1.1k
views
1
answer
Visualizing exome Sequencing data for depth
sequencing written 3.3 years ago by ruhirai20 • updated 19 hours ago by Gungor Budak210
0
votes
0
answers
54
views
0
answers
BGIseq 500 - raw data files
bcl bgi written 16 hours ago by Gennady Khvorykh80
0
votes
0
answers
32
views
0
answers
0
votes
0
answers
30
views
0
answers
8
votes
2
answers
145
views
2
answers
Plotting the expression values for two genes in a range of cells
R ggplot2 written 1 day ago by Za40 • updated 15 hours ago by egeulgen280
0
votes
0
answers
84
views
0
answers
0
votes
1
answer
76
views
1
answer
How to calculate read frequency from raw count data
R rna-seq written 22 hours ago by vkgaur2520 • updated 15 hours ago by Devon Ryan81k
1
vote
0
answers
70
views
0
answers
Trimming reads of Chipseq samples
alignment chip-seq written 1 day ago by GK161030 • updated 15 hours ago by Devon Ryan81k
0
votes
0
answers
48
views
0
answers
p-values in GTEx
gene expression snp written 13 hours ago by kakukeshi20
0
votes
1
answer
75
views
1
answer
4
votes
0
answers
69
views
0
answers
De novo assembly programm
assembly written 12 hours ago by Toto2610
0
votes
0
answers
63
views
0
answers
1
vote
2
answers
107
views
2
answers
0
votes
1
answer
130
views
1
answer
2
votes
1
answer
93
views
1
answer
0
votes
1
answer
685
views
1
answer
4
votes
1
answer
40
views
1
answer
Mapping paired-end reads to a draft genome using HISAT2
genome guided alignment rna-seq hisat2 written 3 hours ago by Farbod3.1k • updated 3 hours ago by genomax50k
0
votes
0
answers
23
views
0
answers
0
votes
2
answers
28
views
2
answers
taxid to genome refseq accession number
genome taxid refseq accession number genome written 2 hours ago by ruchikabhat3130 • updated 1 hour ago by genomax50k
0
votes
0
answers
14
views
0
answers
0
votes
0
answers
14
views
0
answers
0
votes
0
answers
55
views
0
answers
0
votes
1
answer
10
views
1
answer
Genome assembly and annotation
assembly written 48 minutes ago by biodano.geo0 • updated 10 minutes ago by Philipp Bayer5.5k
0
votes
1
answer
65
views
1
answer
Can't find chr1 in a large fasta file using samtools/htsjdk
fasta assembly reference samtools written 13 hours ago by ljw10010 • updated 9 minutes ago by Eric Lim600
2
votes
1
answer
2.0k
views
1
answer
.bam file of human reference genome (hg19)
samtools written 3.4 years ago by Max130 • updated 21 hours ago by Biostar ♦♦ 20
0
votes
0
answers
12
views
0
answers
How to know if a variant is sequencing or mapping artifact?
variant vcf file freebayes written 22 minutes ago by kspata10 • updated 4 minutes ago by finswimmer2.8k
3
votes
0
answers
128
views
0
answers
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