Latest
Open
RNA-Seq
ChIP-Seq
SNP
Assembly
Tutorials
Tools
Jobs
Forum
Planet
All »
Home
Log In
or   Classic search
<prev • 62,994 results • page 1 of 2100 • next >
1
vote
0
answers
100
views
0
answers
blast -seqidlist is slow
blast written 7 weeks ago by gb • 280 • updated 34 minutes ago by Biostar ♦♦ 20
1
vote
0
answers
18
views
0
answers
Efficiently aligning a lot of reads on the same small reference sequence
alignment next-gen written 1 hour ago by cedric.stroobandt • 0
0
votes
0
answers
21
views
0
answers
which gap filler do you recommend?
genome assembly gapfiller written 1 hour ago by Mostafa • 0
0
votes
0
answers
26
views
0
answers
News: Comparative Genomics Workshop (Berlin, 1-5 October 2018). Last Call
news next-gen pacbio written 3 hours ago by carlopecoraro2 • 710
1
vote
0
answers
143
views
0
answers
blast database name in output
blast written 9 weeks ago by gb • 280 • updated 6 hours ago by Biostar ♦♦ 20
11
votes
2
answers
186
views
6 follow
2
answers
Which repository is more appropriate to submit for cancer cell line (bulk) RNA-seq data ?
rna-seq written 10 weeks ago by arta • 520 • updated 12 hours ago by Biostar ♦♦ 20
0
votes
0
answers
45
views
0
answers
How to automatically retrieve genes of preselected enzymes in a pathway map?
gene written 14 hours ago by salamandra • 160
371
votes
17
answers
26k
views
170 follow
17
answers
News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 20 months ago by Istvan Albert ♦♦ 77k • updated 14 hours ago by Fanta • 0
9
votes
0
answers
187
views
6 follow
0
answers
Tool: Introducing Skymap: Allelic read counts extracted from 250,000 human sequencing runs in Sequence Read Archive
chip-seq snp rna-seq tool written 5 days ago by btsui • 170
0
votes
0
answers
44
views
0
answers
Using RepeatModeler for novel assembled genome
genome assembly repeatmodeler written 21 hours ago by nehleen11 • 0 • updated 15 hours ago by WouterDeCoster ♦ 31k
5
votes
1
answer
60
views
1
answer
Difference in FPKM values of lncRNA when using different annotation files
reference annotations gencode written 17 hours ago by piyushjo • 20 • updated 17 hours ago by grant.hovhannisyan • 990
2
votes
1
answer
79
views
1
answer
Estimating the purity of tumor cells in gene expression microarray data
cell purity microarray written 2 days ago by Shamim Sarhadi • 200
4
votes
1
answer
2.3k
views
1
answer
Merging And De-Duplicating Structural Variant Calls (Bedpe)
intersect structural written 7.1 years ago by Stephane Plaisance • 370 • updated 18 hours ago by Biostar ♦♦ 20
1
vote
1
answer
74
views
1
answer
Giga base or Giga byte
gb assembly coverage written 18 hours ago by Shawrob400 • 0
2
votes
1
answer
84
views
1
answer
Know if a pathway is being functionally activated or repressed by a group of up-regulated genes
text-mining rna-seq gene set enrichment written 1 day ago by salamandra • 160 • updated 20 hours ago by Kevin Blighe ♦ 25k
9
votes
1
answer
100
views
1
answer
Forum: How to acknowledge in the paper a reference genome that hasn't been published yet?
paper forum reference written 1 day ago by ciemanek • 100 • updated 20 hours ago by genomax ♦ 54k
2
votes
0
answers
342
views
0
answers
Job: Research Scientist in Biostatistics/Bioinformatics at UNC Charlotte, NC, USA
genomics statistics data science job R ngs written 6 weeks ago by bigmawen • 270
0
votes
1
answer
47
views
1
answer
autosomal ancestry inference
gwas ancestry written 23 hours ago by J.F.Jiang • 710 • updated 21 hours ago by Kevin Blighe ♦ 25k
0
votes
3
answers
947
views
3
answers
RepeatModeler cannot be run in parallel
repeatmodeler repeatmasker written 23 months ago by tlorin • 240 • updated 21 hours ago by nehleen11 • 0
0
votes
1
answer
109
views
1
answer
How group merged VCFs in one GT column
vcf bcftools written 1 day ago by miqrom • 0 • updated 22 hours ago by Kevin Blighe ♦ 25k
0
votes
0
answers
38
views
0
answers
annotate and analyse mutation from cosmic
assembly chip-seq mutation annotation written 22 hours ago by sahhomaha • 0
4
votes
1
answer
125
views
5 follow
1
answer
Very low unique mapped reads - STAR alignment
rna-seq written 1 day ago by junsionglow • 20 • updated 23 hours ago by h.mon ♦ 18k
0
votes
0
answers
49
views
0
answers
remove primer sequences from BAM file
bam primer written 23 hours ago by J.F.Jiang • 710
2
votes
0
answers
91
views
0
answers
Forum: TACC vs SDSC vs HTCondor
forum pbs written 21 days ago by Shicheng Guo • 6.1k • updated 23 hours ago by h.mon ♦ 18k
4
votes
0
answers
138
views
5 follow
0
answers
Issue with Samtools variant calling
genome assembly alignment written 7 weeks ago by williamsbrian5064 • 90 • updated 1 day ago by Biostar ♦♦ 20
4
votes
2
answers
114
views
2
answers
Identifying covered genes from nanopore cDNA-seq reads
gene alignment rna-seq written 1 day ago by florian.bernard5 • 10 • updated 1 day ago by WouterDeCoster ♦ 31k
0
votes
0
answers
821
views
0
answers
How to detect segmental duplications?
genome assembly alignment written 23 months ago by lamz138138 • 40 • updated 1 day ago by WouterDeCoster ♦ 31k
4
votes
4
answers
143
views
5 follow
4
answers
How to get PCA3 and PCA4 from Deseq2?
rna-seq written 1 day ago by morteza.khabiri • 0 • updated 1 day ago by cpad0112 • 8.3k
0
votes
0
answers
32
views
0
answers
Extracting similar ssrs from two different misa files
perl python misa rna-seq ssrs written 1 day ago by kartikayprasad • 10
0
votes
1
answer
50
views
1
answer
VCF to Bed file format using GATK
vcf gatk rna-seq bed written 1 day ago by Sa • 0 • updated 1 day ago by chrchang523 ♦ 3.7k
<prev • 62,994 results • page 1 of 2100 • next >
Recent Votes
Recent Locations • All »
  • Brazil, just now
  • United Kingdom, 6 minutes ago
  • Belgium, 17 minutes ago
  • United Kingdom, 17 minutes ago
Recent Awards • All »
Recent Replies
Content
Help
Access
Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 716 users visited in the last hour