Latest
Open
RNA-Seq
ChIP-Seq
SNP
Assembly
Tutorials
Tools
Jobs
Forum
Planet
All »
Home
Log In
or   Classic search
<prev • 60,912 results • page 1 of 2031 • next >
0
votes
2
answers
608
views
2
answers
ChIP-nexus peak call
chip-seq written 20 months ago by Sudhir Jadhao • 50 • updated 2 minutes ago by mlweilert • 0
0
votes
0
answers
18
views
0
answers
Please suggest an appropriate genome-guided transcriptome assembler
genome marker alignment rna-seq written 49 minutes ago by seta • 980
0
votes
1
answer
37
views
1
answer
How To Split Vcf Files
vcf vcftools written 1 hour ago by mayara_salvian • 0 • updated 1 hour ago by Pierre Lindenbaum ♦ 108k
0
votes
1
answer
33
views
1
answer
How to link "miRNA gene quantification" and "clinical- Patient" data retrieved from TCGA
contrast tcga mirnaseq edger written 8 hours ago by Björn • 20 • updated 1 hour ago by Kevin Blighe ♦ 21k
0
votes
0
answers
20
views
0
answers
How to align the sanger sequenced fragments against human reference gene?
dnaseq alignment align sanger written 1 hour ago by bioinforesearchquestions • 140
0
votes
1
answer
33
views
1
answer
Blastn Gives Different Results Based on Database Size
alignment sequence blast written 2 hours ago by khv • 0 • updated 1 hour ago by lieven.sterck • 1.6k
0
votes
1
answer
37
views
1
answer
the bam file used for Diffbind
R chip-seq sequencing written 2 hours ago by mikysyc2016 • 10 • updated 1 hour ago by jared.andrews07 • 730
352
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 1 hour ago by Vijay Lakhujani ♦ 2.5k
2
votes
0
answers
46
views
0
answers
News: GeNets: a unified web platform for network-based genomic analyses
pathways news visualization networks rna-seq written 3 hours ago by vchris_ngs • 4.5k • updated 2 hours ago by genomax ♦ 49k
0
votes
0
answers
50
views
0
answers
DSK: readme and options
gatb written 4 hours ago by sebastien.letort • 40
0
votes
1
answer
36
views
1
answer
Samtools mpileup returns empty vcf file
samtools mpileup written 3 hours ago by shreyasibiswas88 • 30 • updated 2 hours ago by Ram ♦ 15k
0
votes
0
answers
1.1k
views
0
answers
drawing comparison gene maps between strains- synterny diagrams
gene software error sequence written 3.4 years ago by mwanerhi erfgtr • 30 • updated 2 hours ago by Biostar ♦♦ 20
1
vote
0
answers
53
views
0
answers
Can we concatenate two fastq files from same sample but different runs
rna-seq sequencing written 3 hours ago by Payal • 30
0
votes
1
answer
40
views
1
answer
weird problem with summit.bed file from macs2
software error peak calling chip-seq sequencing written 5 hours ago by mikysyc2016 • 10 • updated 3 hours ago by jared.andrews07 • 730
0
votes
0
answers
33
views
0
answers
SNP + INDEL Merging Guidelines
vcf indel snp merging written 3 hours ago by QVINTVS_FABIVS_MAXIMVS • 2.1k
0
votes
0
answers
38
views
0
answers
Tool to do Variant calling from contigs data
variant calling contigs written 4 hours ago by de.mecquenem.ninon • 0
4
votes
1
answer
61
views
1
answer
Remove columns from the VCF file using vcftools
vcftools written 4 hours ago by mayara_salvian • 0 • updated 4 hours ago by genomax ♦ 49k
1
vote
1
answer
54
views
1
answer
most sequenced genomes
genomes microbial written 5 hours ago by savscosta • 0 • updated 4 hours ago by genomax ♦ 49k
1
vote
1
answer
238
views
1
answer
Classify cells using seurat
monocle scrna seurat written 3 months ago by AB • 90 • updated 5 hours ago by dppb05 • 40
0
votes
0
answers
28
views
0
answers
Population genetic inference from pooled-DNA microsatellite genotyping
R microsatellites pooled dna written 5 hours ago by apaspati • 0
10
votes
2
answers
211
views
9 follow
2
answers
News: #NGSchool2018 summer school in bioinformatics
news ngschool nanopore personalised medicine written 14 days ago by kzkedzierska • 110
0
votes
1
answer
56
views
1
answer
What modern free software can compute CODIS STR and other forensic biomarkers from the input FASTQ human complete or a partial genome file?
software str forensic fastq biomarkers written 7 hours ago by bioinformatics_dublin • 0 • updated 7 hours ago by pfs • 230
0
votes
1
answer
66
views
1
answer
Perform of disco Snp with low coverage samples
discosnp snp calling low coverage written 7 days ago by shinken123 • 50 • updated 7 hours ago by pierre.peterlongo • 760
3
votes
0
answers
112
views
7 follow
0
answers
How to compare 2 pine transcriptome fasta contigs without mapping to a reference or annotating against databases?
annotation contig comparision pine transcriptome written 12 hours ago by bioinformatics_dublin • 0
3
votes
1
answer
48
views
1
answer
How to combine chromosome vcf files
genome assembly next-gen alignment written 7 hours ago by williamsbrian5064 • 60 • updated 7 hours ago by Pierre Lindenbaum ♦ 108k
3
votes
1
answer
71
views
1
answer
How to map viral RNA from human blood samples?
metagenomics mapping virus written 12 hours ago by caggtaagtat • 200
0
votes
0
answers
43
views
0
answers
Picard ExtractIlluminaBarcodes error
picard extractilluminabarcodes demultiplex written 8 hours ago by mark.rose • 10
0
votes
0
answers
59
views
0
answers
FeatureCounts summarizing at exon level
featurecounts rna-seq exon written 8 hours ago by yamar • 0
11
votes
2
answers
152
views
2
answers
Get every variables sites between two aligned CDS sequences
non-synonymous alignment mutation synonymous written 4 days ago by maxime.policarpo • 20 • updated 8 hours ago by finswimmer ♦ 2.7k
0
votes
0
answers
106
views
0
answers
which tool I can use to defined varying-size, equal-coverage chromosomal windows
genome chip-seq sequencing written 9 weeks ago by weiyanjia2008 • 0 • updated 8 hours ago by Biostar ♦♦ 20
<prev • 60,912 results • page 1 of 2031 • next >
Recent Votes
Recent Locations • All »
  • United Kingdom, 1 minute ago
  • Seattle,WA, USA, 1 minute ago
  • Brazil, 2 minutes ago
  • Canada, 5 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: 1494 users visited in the last hour