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0
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0
replies
5.0k
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Comment:
Comment: How to use htseq-count with several samples ?
3.0 years ago by
VBer
▴ 200
0
votes
0
replies
1.2k
views
Comment:
C: Visualization of fold changes of candidate genes as heatmap across multiple inde
4.0 years ago by
VBer
▴ 200
1
vote
1
reply
2.4k
views
Comment:
C: Mann-Whitney Test/Wilcoxon but for individual genes between case and control
4.0 years ago by
VBer
▴ 200
1
vote
2
replies
1.2k
views
Visualization of fold changes of candidate genes as heatmap across multiple independent experiments
RNA-Seq
Visualization
HeatMap
Meta-analysis
4.0 years ago by
VBer
▴ 200
0
votes
0
replies
2.4k
views
Comment:
C: Mann-Whitney Test/Wilcoxon but for individual genes between case and control
4.1 years ago by
VBer
▴ 200
2
votes
10
replies
2.4k
views
Mann-Whitney Test/Wilcoxon but for individual genes between case and control
RNA-Seq
Statistics
4.1 years ago by
VBer
▴ 200
0
votes
1
reply
868
views
Comment:
C: How to make KEGG plots based on the gene list with KO ID
4.1 years ago by
VBer
▴ 200
0
votes
1
reply
2.4k
views
Comment:
C: Mann-Whitney Test/Wilcoxon but for individual genes between case and control
4.1 years ago by
VBer
▴ 200
0
votes
0
replies
2.4k
views
Comment:
C: Mann-Whitney Test/Wilcoxon but for individual genes between case and control
4.1 years ago by
VBer
▴ 200
0
votes
1
reply
2.4k
views
Comment:
C: Mann-Whitney Test/Wilcoxcon but for individual genes between case and control
4.1 years ago by
VBer
▴ 200
1
vote
0
replies
926
views
Comment:
C: Methodology: Meta-analysis and integration of published transcriptomics and prot
4.2 years ago by
VBer
▴ 200
0
votes
0
replies
1.2k
views
Comment:
C: Hypergeometric test on gene lists
4.2 years ago by
VBer
▴ 200
0
votes
0
replies
17k
views
Comment:
C: Justifying Learning Linux For Bioinformatics
4.3 years ago by
VBer
▴ 200
1
vote
1
reply
926
views
Methodology: Meta-analysis and integration of published transcriptomics and proteomics data
RNA-Seq
proteomics
omics
4.3 years ago by
VBer
▴ 200
0
votes
0
replies
2.2k
views
Comment:
C: Possible reasons mapping percentage abysmally low for miRNA reads?
4.3 years ago by
VBer
▴ 200
0
votes
2
replies
3.1k
views
What is the importance of checking per base sequence content and per sequence GC content during Quality Control of NGS reads?
fastqc
next-gen
sequencing
updated 4.6 years ago by
Biostar
20 • written 5.6 years ago by
VBer
▴ 200
2
votes
1
reply
2.7k
views
Calculating genetic distance from VCF to MAP format
population genomics
updated 4.6 years ago by
chrchang523
11k • written 4.6 years ago by
VBer
▴ 200
1
vote
0
replies
1.3k
views
Comment:
C: blastn of reference genome CDS to subject genome gives range of hits, which do n
4.6 years ago by
VBer
▴ 200
0
votes
1
reply
1.3k
views
Comment:
C: blastn of reference genome CDS to subject genome gives range of hits, which do n
4.7 years ago by
VBer
▴ 200
0
votes
1
reply
1.3k
views
Comment:
C: blastn of reference genome CDS to subject genome gives range of hits, which do n
4.7 years ago by
VBer
▴ 200
4
votes
6
replies
1.3k
views
blastn of reference genome CDS to subject genome gives range of hits, which do not translate into protein
BLAST
4.7 years ago by
VBer
▴ 200
0
votes
0
replies
2.2k
views
Comment:
C: Possible reasons mapping percentage abysmally low for miRNA reads?
4.7 years ago by
VBer
▴ 200
7
votes
9
replies
2.2k
views
Possible reasons mapping percentage abysmally low for miRNA reads?
miRNA
miRDeep2
4.9 years ago by
VBer
▴ 200
1
vote
2
replies
2.2k
views
Comment:
C: Possible reasons mapping percentage abysmally low for miRNA reads?
4.9 years ago by
VBer
▴ 200
1
vote
1
reply
2.2k
views
Comment:
C: Possible reasons mapping percentage abysmally low for miRNA reads?
4.9 years ago by
VBer
▴ 200
0
votes
1
reply
2.1k
views
Comment:
C: NOISeq Fold Change calculation seems off?
4.9 years ago by
VBer
▴ 200
3
votes
3
replies
2.1k
views
NOISeq Fold Change calculation seems off?
RNA-Seq
updated 4.9 years ago by
Hyper_Odin
▴ 320 • written 5.4 years ago by
VBer
▴ 200
0
votes
0
replies
1.7k
views
Comment:
C: Remove homozygous reference SNPS present in ALL samples of multi-sample VCF file
5.0 years ago by
VBer
▴ 200
1
vote
3
replies
1.7k
views
Remove homozygous reference SNPS present in ALL samples of multi-sample VCF file
vcf
5.0 years ago by
VBer
▴ 200
0
votes
0
replies
2.2k
views
Comment:
C: getting sequence by combining reference and variants (fasta and vcf files)
5.3 years ago by
VBer
▴ 200
0
votes
0
replies
7.1k
views
Comment:
C: Emboss seqret - problem conversion gff+fasta to EMBL
5.3 years ago by
VBer
▴ 200
1
vote
0
replies
4.1k
views
Comment:
C: Hard time trying to calculate Allele Frequency and DP from Platypus
5.3 years ago by
VBer
▴ 200
0
votes
0
replies
1.3k
views
Comment:
C: Bioinformatics Project this summer
5.4 years ago by
VBer
▴ 200
1
vote
0
replies
1.1k
views
Answer:
A: Coverage of exome
5.4 years ago by
VBer
▴ 200
1
vote
0
replies
26k
views
Answer:
A: Variant call format (VCF) file, how to get statistics per sample?
5.4 years ago by
VBer
▴ 200
0
votes
0
replies
3.3k
views
Comment:
C: Problem in running NOISeq-sim
5.4 years ago by
VBer
▴ 200
2
votes
0
replies
5.8k
views
Comment:
C: bcftools mpileup --max depth : What would be a reasonable setting for this optio
5.4 years ago by
VBer
▴ 200
1
vote
0
replies
6.9k
views
Comment:
C: how is the output of bcftools stats calculated?
5.4 years ago by
VBer
▴ 200
1
vote
0
replies
2.4k
views
Comment:
C: bcftools stats numbers do not match
5.4 years ago by
VBer
▴ 200
1
vote
1
reply
2.4k
views
bcftools stats numbers do not match
bcftools
5.4 years ago by
VBer
▴ 200
1
vote
8
replies
6.8k
views
Error using feature counts with DESeq2 : Cannot create DESeqData object
RNA-Seq
DESeq2
featurecounts
updated 5.5 years ago by
Biostar
20 • written 5.6 years ago by
VBer
▴ 200
0
votes
1
reply
5.8k
views
Comment:
C: bcftools mpileup --max depth : What would be a reasonable setting for this optio
5.6 years ago by
VBer
▴ 200
7
votes
4
replies
5.8k
views
bcftools mpileup --max depth : What would be a reasonable setting for this option?
bcftools
mpileup
consensus
5.6 years ago by
VBer
▴ 200
0
votes
0
replies
6.8k
views
Comment:
C: Error using feature counts with DESeq2 : Cannot create DESeqData object
5.6 years ago by
VBer
▴ 200
0
votes
1
reply
6.8k
views
Comment:
C: Error using feature counts with DESeq2 : Cannot create DESeqData object
5.6 years ago by
VBer
▴ 200
0
votes
1
reply
6.8k
views
Comment:
C: Error using feature counts with DESeq2 : Cannot create DESeqData object
5.6 years ago by
VBer
▴ 200
0
votes
0
replies
4.0k
views
Comment:
C: BQSR vs VQSR
5.6 years ago by
VBer
▴ 200
0
votes
0
replies
3.1k
views
Comment:
C: What is the importance of checking per base sequence content and per sequence GC
5.6 years ago by
VBer
▴ 200
8
votes
2
replies
6.5k
views
Why do we need a .fai file and a .dict file of the reference during alignment and variant calling using GATK?
next-gen
sequencing
GATK
alignment
file_formats
updated 5.6 years ago by
Pierre Lindenbaum
164k • written 5.6 years ago by
VBer
▴ 200
3
votes
1
reply
2.4k
views
What is a Chimera with regards to NGS?
ngs
next-gen
sequencing
5.6 years ago by
VBer
▴ 200
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