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2
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SNPs genomic classification based on VCF annotation
R snp written 23 hours ago by aarvaBioinfo • 10
1
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0
answers
115
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0
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IGV empty tracks render in blue
cnv igv written 26 days ago by roy.granit • 740 • updated 1 hour ago by Biostar ♦♦ 20
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24
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Forum: Computation-Intesive Application in the field of bioinformatics
software forum application computation-intensive written 2 hours ago by mostafa.hadadian • 0 • updated 1 hour ago by h.mon ♦ 18k
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1
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39
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1
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Differences between parSeqSim and twoSeqSim results
R sequence similarity protr written 16 hours ago by lefthandgergo • 0 • updated 1 hour ago by h.mon ♦ 18k
0
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1
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111
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1
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Help interpreting Stringtie 'fully covered transcripts' output
assembly rna-seq written 9 weeks ago by freuv • 20 • updated 2 hours ago by h.mon ♦ 18k
1
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1
answer
70
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1
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htseq-count error utf-8 codec can't decode
htseq-count rna-seq written 11 hours ago by alexadeanfitz • 0
0
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0
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21
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0
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How to do differential peak analysis after scaling BAM files
chip-seq written 2 hours ago by xiaoyonf • 0
1
vote
1
answer
50
views
1
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Directionality of KEGG/Reactome/Wikipathways
pathways wikipathways reactome kegg written 4 hours ago by g.e.novakovsky • 10 • updated 3 hours ago by h.mon ♦ 18k
373
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17
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27k
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172 follow
17
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 20 months ago by Istvan Albert ♦♦ 77k • updated 3 hours ago by Fanta • 0
0
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1
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115
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6 follow
1
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Forum: Search for gene variants
forum next-gen written 9 hours ago by Rm ♦ 7.7k • updated 4 hours ago by jared.andrews07 • 870
4
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2
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2.6k
views
2
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Check if REF allele is minor allele in any variant
ref variant minor allele written 3.8 years ago by Ram ♦ 17k • updated 4 hours ago by Shicheng Guo • 6.1k
10
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0
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250
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6 follow
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Tool: Introducing Skymap: Allelic read counts extracted from 250,000 human sequencing runs in Sequence Read Archive
chip-seq snp rna-seq tool written 8 days ago by btsui • 230
2
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1
answer
105
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1
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Differential expression analysis of normalized expression of RNA seq data
rna-seq written 12 days ago by Javad • 20 • updated 6 hours ago by b.nota ♦ 4.6k
6
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2
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77
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Parsing large sequence file into per-sample files after barcodes/primers removed.
dereplicate written 9 hours ago by caverill • 40 • updated 8 hours ago by finswimmer ♦ 4.5k
1
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0
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57
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mice whole genome sequencing Analysis
assembly next-gen sequence alignment sequencing written 8 hours ago by tarekzakaria.badr • 0
1
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2
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179
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Difference between differential transcript expression and differential splicing
splicing expression transcript written 7 days ago by sneha108ss • 0 • updated 9 hours ago by Charles Warden ♦ 5.1k
0
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1
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69
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1
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GWAS: how do we know we have the most appropriate model?
gwas genomic control inflation gc statistics written 15 hours ago by Nick • 40 • updated 9 hours ago by Kevin Blighe ♦ 26k
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41
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Transition and transversion as a quality of SNP call set
transition snp written 9 hours ago by hpapoli • 60
0
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1
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32
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1
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how to get circRNA fasta sequence from CIRI bed
circrna analysis written 10 hours ago by fanyucai1 • 0 • updated 9 hours ago by Kevin Blighe ♦ 26k
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36
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0
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Using mmseq expression data for analysis/classification
mmseq rna-seq written 10 hours ago by Li • 0
0
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38
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multiIntersectBed Error: The requested bed file could not be opened. Exiting!
genome bedtools multiintersectbed written 10 hours ago by yren0429 • 0
4
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1
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74
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1
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BLAST based on 100k sequences rnaseq?
rna-seq blast written 12 hours ago by heydt.mathias • 0
0
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0
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35
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How to set 1Kb resolution for Hi-C Juicebox Visualization
next-gen chip-seq written 12 hours ago by harikrishnanc903 • 0
0
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0
answers
51
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News: Course: Introduction to Python
python news next-gen programming written 12 hours ago by carlopecoraro2 • 710
1
vote
1
answer
73
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5 follow
1
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Batch pairwise alignment and consensus
alignment written 13 hours ago by lewis272727 • 0 • updated 12 hours ago by Michael Dondrup ♦ 44k
0
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72
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DESeq2 using samples with different unique alignment rates
R rna-seq written 13 hours ago by Tash • 0
12
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2
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114
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5 follow
2
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Comparing reads of multiple BAM files (using getopts for parsing)
bam samtools seqtl getopts written 13 hours ago by m93 • 50 • updated 13 hours ago by jrj.healey ♦ 6.1k
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36
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How to find key apoptotic markers across subtypes of a colorectal cancer dataset?
R cancer apoptotic subtypes markers written 14 hours ago by bio94 • 40
4
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1
answer
115
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1
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deseq2 foldchange issue
rna-seq written 19 hours ago by krushnach80 • 320
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Job: Bioinformatician & Software Developer at Wellcome Centre for Molecular Parasitology, Glasgow, UK
software developer job bioinformatician written 14 hours ago by Sej Modha ♦ 3.4k
<prev • 49 results • page 1 of 2 • next >
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