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2
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618
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Comment: Comment: Distribution of assayed SNPs per sample
26 days ago by mbyvcm ▴ 480
0
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0
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933
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Comment: Comment: Different comparisons in RNASeq Analysis
27 days ago by mbyvcm ▴ 480
0
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0
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933
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Comment: Comment: Different comparisons in RNASeq Analysis
4 weeks ago by mbyvcm ▴ 480
0
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1
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618
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Comment: Comment: Distribution of assayed SNPs per sample
4 weeks ago by mbyvcm ▴ 480
0
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2
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933
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Answer: Answer: Different comparisons in RNASeq Analysis
4 weeks ago by mbyvcm ▴ 480
0
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2
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978
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Comment: Comment: Proposal on CNV (Copies Variants Numer) analysis tools
6 weeks ago by mbyvcm ▴ 480
0
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0
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926
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Answer: Answer: RNAseq meta-analysis to identify “consistently expressed” genes
7 weeks ago by mbyvcm ▴ 480
0
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1
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602
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Comment: Comment: TCGA Germline allelic fraction distribution
7 weeks ago by mbyvcm ▴ 480
1
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0
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825
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Answer: Answer: Does comparing two different groups to a common third group introduce bias in th
14 months ago by mbyvcm ▴ 480
0
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0
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1.2k
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Answer: Answer: Introduce SNPs on FASTA
14 months ago by mbyvcm ▴ 480
0
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0
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588
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Comment: Comment: Finding batch and outlayers
14 months ago by mbyvcm ▴ 480
1
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0
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2.7k
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Answer: A: Why is it important to control ethnicity when studying rare variants?
updated 5.5 years ago by 45k • written 9.4 years ago by ▴ 480
0
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0
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3.5k
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Comment: C: How to remove the high correlated SNPs in R
updated 5.5 years ago by 45k • written 9.4 years ago by ▴ 480
0
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1
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3.5k
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Answer: A: How to remove the high correlated SNPs in R
updated 5.5 years ago by 45k • written 9.5 years ago by ▴ 480
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0
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3.3k
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Answer: A: Set-based test - PLINK
updated 5.5 years ago by 45k • written 9.5 years ago by ▴ 480
0
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0
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3.9k
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Comment: C: Velvet Assembly Parameters
updated 5.5 years ago by 45k • written 9.5 years ago by ▴ 480
0
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0
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4.1k
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Comment: Comment: Plink: how to recode SNP identifiers
updated 5.5 years ago by 45k • written 9.5 years ago by ▴ 480
1
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2
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4.1k
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Answer: A: Plink: how to recode SNP identifiers
updated 5.5 years ago by 45k • written 9.5 years ago by ▴ 480
0
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0
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1.3k
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Answer: A: Find region that full captures association signal
6.2 years ago by mbyvcm ▴ 480
7
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3
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2.7k
views
pythonic equivalent to reduce() in R GRanges - how to collapse ranged data?
R python
updated 6.3 years ago by ▴ 980 • written 7.4 years ago by ▴ 480
3
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0
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3.0k
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Answer: A: Change plink file for logistic in R
updated 6.8 years ago by 45k • written 9.4 years ago by ▴ 480
1
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0
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1.5k
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Job: Clinical Bioinformatician (University Hospital of Wales, Cardiff, UK)
clinical-bioinformatics NGS
updated 2.3 years ago by 45k • written 6.9 years ago by ▴ 480
0
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0
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2.7k
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Comment: C: pythonic equivalent to reduce() in R GRanges - how to collapse ranged data?
7.4 years ago by mbyvcm ▴ 480
0
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1
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2.1k
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Comment: C: Sorting the haplotypes by similarities of SNPs in R
7.4 years ago by mbyvcm ▴ 480
0
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0
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1.3k
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Answer: A: Parsing Coding Seq w grep
7.4 years ago by mbyvcm ▴ 480
1
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1
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6.3k
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Comment: C: mapping between gene symbol and entrez ID
7.4 years ago by mbyvcm ▴ 480
2
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0
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8.4k
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Answer: A: Loading PLINK files to Haploview
7.5 years ago by mbyvcm ▴ 480
0
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0
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2.4k
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Comment: C: Ranking of genes in multiple samples
7.5 years ago by mbyvcm ▴ 480
0
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1
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2.4k
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Comment: C: Ranking of genes in multiple samples
7.5 years ago by mbyvcm ▴ 480
0
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1
reply
2.7k
views
Comment: C: gTEX normalize counts by genotype
7.6 years ago by mbyvcm ▴ 480
0
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1
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3.2k
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Answer: A: Gene synonyms/aliases - Is there a way to collect them programmatically
7.7 years ago by mbyvcm ▴ 480
0
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0
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3.3k
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Answer: A: p-value and FDR
7.7 years ago by mbyvcm ▴ 480
0
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0
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2.6k
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Answer: A: Bacterial genome annotation
7.8 years ago by mbyvcm ▴ 480
0
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0
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2.4k
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Comment: C: A confusion regarding haplotype
7.8 years ago by mbyvcm ▴ 480
1
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0
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2.4k
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Answer: A: A confusion regarding haplotype
7.8 years ago by mbyvcm ▴ 480
0
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1
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2.4k
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Comment: C: A confusion regarding haplotype
7.8 years ago by mbyvcm ▴ 480
1
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1
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3.5k
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Comment: C: Problem with LARGE MATRIX
7.9 years ago by mbyvcm ▴ 480
1
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0
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2.3k
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Answer: A: PCR : genes vs pseudogenes
7.9 years ago by mbyvcm ▴ 480
2
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1
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3.7k
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Answer: A: Help with Fisher test between drug-targets
7.9 years ago by mbyvcm ▴ 480
0
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1
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3.7k
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Comment: C: Help with Fisher test between drug-targets
7.9 years ago by mbyvcm ▴ 480
0
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1
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3.6k
views
Comment: C: plink epistasis result
8.5 years ago by mbyvcm ▴ 480
0
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0
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3.6k
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Comment: C: plink epistasis result
8.5 years ago by mbyvcm ▴ 480
0
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0
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5.8k
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Answer: A: Replace vcf in-house variant IDs with dnSNP variant IDs
8.5 years ago by mbyvcm ▴ 480
0
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0
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3.8k
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Comment: C: Require help in using PLINK flags and scripts
8.5 years ago by mbyvcm ▴ 480
0
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0
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1.7k
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Answer: A: PLINK- chromosome ID disappears after running association tests
8.5 years ago by mbyvcm ▴ 480
3
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1
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2.6k
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Answer: A: Is there a quick method to extract regularly-spaced features/SNPs from a VCF fil
8.5 years ago by mbyvcm ▴ 480
0
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0
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1.6k
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Comment: C: finding the gene contain the snps ID
8.5 years ago by mbyvcm ▴ 480
3
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1
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1.6k
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Answer: A: finding the gene contain the snps ID
8.5 years ago by mbyvcm ▴ 480
2
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0
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3.3k
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Comment: C: Help with NGS analysis
8.5 years ago by mbyvcm ▴ 480
1
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1
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3.7k
views
Answer: C: merging plink files
8.5 years ago by mbyvcm ▴ 480
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