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Answer: Answer: Effect of unequal sample sizes on p-value
2.7 years ago by German.M.Demidov ★ 2.9k
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1.9k
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Answer: Answer: Inferring CNVs from BAM files with SAMTools depth
2.7 years ago by German.M.Demidov ★ 2.9k
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498
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Answer: Answer: Simple question about deleted genes in TCGA CNV level 3 data
2.9 years ago by German.M.Demidov ★ 2.9k
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1.7k
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Answer: Answer: Cons of Smith-Waterman Alignment
2.9 years ago by German.M.Demidov ★ 2.9k
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1.8k
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Answer: Answer: Genetic Variants in NGS analysis
2.9 years ago by German.M.Demidov ★ 2.9k
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2.6k
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Answer: Answer: Deseq same padj values for a lot of genes but with different p-values
3.0 years ago by German.M.Demidov ★ 2.9k
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1
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1.3k
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Answer: Answer: Need suggestions to combine the missense variants pathogenicity prediction score
3.0 years ago by German.M.Demidov ★ 2.9k
2
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1
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2.2k
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Answer: Answer: How do I interpret a 200bp reduction of coverage in a gene exon?
3.0 years ago by German.M.Demidov ★ 2.9k
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2.1k
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Answer: Answer: Important genes are not differentially expressed
3.1 years ago by German.M.Demidov ★ 2.9k
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1.6k
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Answer: Comment: GWAS Summary statistic
3.1 years ago by German.M.Demidov ★ 2.9k
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1.8k
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Answer: A: Problem in understanding False Discovery Rate (FDR)
3.4 years ago by German.M.Demidov ★ 2.9k
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1.4k
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Answer: C: How to astimate the copy number of sex chromosome using QDNAseq or other tools (
3.6 years ago by German.M.Demidov ★ 2.9k
2
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914
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Answer: C: correlation pearson and spearman PValue
3.7 years ago by German.M.Demidov ★ 2.9k
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1.2k
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Answer: C: ACMG 59 genes
3.8 years ago by German.M.Demidov ★ 2.9k
2
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1
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1.0k
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Answer: A: Russian universities for the study of biomedicine
3.8 years ago by German.M.Demidov ★ 2.9k
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3.3k
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Answer: A: benchmarking/validation tools for CNVs
3.8 years ago by German.M.Demidov ★ 2.9k
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1.0k
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Answer: A: tool for the new protocol of WES for CNV detection
4.2 years ago by German.M.Demidov ★ 2.9k
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669
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Answer: C: How to smooth methylation data
4.2 years ago by German.M.Demidov ★ 2.9k
2
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1
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1.2k
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Answer: C: Considering only a handful of genes of a priori interest (RNA seq), is it legiti
4.2 years ago by German.M.Demidov ★ 2.9k
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855
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Answer: A: Chromatin states in human neurons?
4.3 years ago by German.M.Demidov ★ 2.9k
2
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1
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981
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Answer: C: DEG, wilcoxon, p value adjustment
4.3 years ago by German.M.Demidov ★ 2.9k
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922
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Answer: C: chip seq peaks are very long
4.3 years ago by German.M.Demidov ★ 2.9k
3
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908
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Answer: C: Need some resources for High Throughput data analysis
4.3 years ago by German.M.Demidov ★ 2.9k
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1.2k
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Answer: C: Tool for CNV benchmarking vs gold standards
4.4 years ago by German.M.Demidov ★ 2.9k
3
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1
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1.1k
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Answer: C: No mutations or copy number alterations was detected in stage I of cancer
4.4 years ago by German.M.Demidov ★ 2.9k
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873
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Answer: A: Plotting - Coverage Analysyis
4.4 years ago by German.M.Demidov ★ 2.9k
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1
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1.3k
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Answer: C: Why can we still be able to continously discover new cancer driver bioinformatic
4.4 years ago by German.M.Demidov ★ 2.9k
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1
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1.5k
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Answer: C: dplyr filter not filtering properly
4.4 years ago by German.M.Demidov ★ 2.9k
2
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1
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1.2k
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Answer: C: DNAcopy plot error
4.4 years ago by German.M.Demidov ★ 2.9k
3
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1
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767
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Answer: A: Breast Cancer updated dataset from free softwares
4.5 years ago by German.M.Demidov ★ 2.9k
1
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1
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909
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Answer: C: Significance of Clusters
4.5 years ago by German.M.Demidov ★ 2.9k
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1
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1.1k
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Answer: C: how to use glm function to predict the factor in value
4.5 years ago by German.M.Demidov ★ 2.9k
3
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1
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2.3k
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Answer: C: NaN in Z.score data from TCGA
4.5 years ago by German.M.Demidov ★ 2.9k
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0
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1.2k
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Answer: C: fdr to p-value
updated 4.6 years ago by 11k • written 4.6 years ago by ★ 2.9k
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1.2k
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Answer: A: Enrichment platforms for 1000GP exome data
5.5 years ago by German.M.Demidov ★ 2.9k
3
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1
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2.2k
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Answer: A: Inconsistent Coverage on X chromosome between genders
6.4 years ago by German.M.Demidov ★ 2.9k
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