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6
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3.7k
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Answer: Answer: hypergeometric distribution for proximal gene enrichment
updated 3.1 years ago by 45k • written 10.2 years ago by 4.8k
0
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1
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3.7k
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Comment: Comment: hypergeometric distribution for proximal gene enrichment
updated 3.1 years ago by 45k • written 10.2 years ago by 4.8k
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0
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2.7k
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Comment: C: How to determine the density and mean of features in specified intervals?
10.2 years ago by LauferVA 4.8k
0
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1
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2.7k
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Answer: Answer: How to determine the density and mean of features in specified intervals?
updated 3.2 years ago by 45k • written 10.2 years ago by 4.8k
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0
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2.6k
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Comment: C: Assessing diversity of random oligonucleotides
10.2 years ago by LauferVA 4.8k
0
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0
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3.0k
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Answer: Answer: Loading IMPUTE2 dosage data into plink/seq
updated 3.4 years ago by 45k • written 10.2 years ago by 4.8k
1
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1
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2.6k
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Comment: C: Assessing diversity of random oligonucleotides
10.2 years ago by LauferVA 4.8k
1
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1
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2.6k
views
Answer: Answer: Assessing diversity of random oligonucleotides
updated 3.1 years ago by 45k • written 10.2 years ago by 4.8k
0
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0
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7.0k
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Comment: C: PLINK does not uncompress GZ file automatically, why?
10.2 years ago by LauferVA 4.8k
0
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0
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2.4k
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Answer: Answer: Database that has all known proteins associated with a particular PFAM or TIGRFA
updated 3.1 years ago by 45k • written 10.2 years ago by 4.8k
0
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1
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13k
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Comment: C: Copy number variation plot (R package)
10.2 years ago by LauferVA 4.8k
1
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1
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3.4k
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Comment: C: LD Analysis between SNPs and CNVs
10.2 years ago by LauferVA 4.8k
3
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1
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3.4k
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Answer: Answer: LD Analysis between SNPs and CNVs
updated 3.1 years ago by 45k • written 10.2 years ago by 4.8k
0
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0
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6.0k
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Comment: C: Hardy-Weinberg assumptions in variant calling
10.3 years ago by LauferVA 4.8k
0
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1
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5.1k
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Comment: Comment: ADMIXTURE results - how can I determine what SNPs are associated with different
updated 3.1 years ago by 45k • written 10.3 years ago by 4.8k
2
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0
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6.0k
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Comment: Comment: Hardy-Weinberg assumptions in variant calling
updated 3.1 years ago by 45k • written 10.3 years ago by 4.8k
0
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0
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2.5k
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Comment: C: SNP and Haplotype differentiation
10.3 years ago by LauferVA 4.8k
0
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0
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2.5k
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Answer: Answer: SNP and Haplotype differentiation
updated 3.1 years ago by 45k • written 10.3 years ago by 4.8k
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0
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2.5k
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Comment: C: SNP and Haplotype differentiation
10.3 years ago by LauferVA 4.8k
4
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1
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6.0k
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Answer: Answer: Hardy-Weinberg assumptions in variant calling
updated 3.1 years ago by 45k • written 10.3 years ago by 4.8k
0
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1
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4.9k
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Comment: C: Availability of a robust, annotation-aware vcf-to-json converter
10.3 years ago by LauferVA 4.8k
1
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1
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4.9k
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Answer: Answer: Availability of a robust, annotation-aware vcf-to-json converter
updated 3.1 years ago by 45k • written 10.3 years ago by 4.8k
0
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0
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2.8k
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Comment: Comment: Patient Clustering Methods for Complex Phenotype GWAS studies
updated 3.1 years ago by 45k • written 10.3 years ago by 4.8k
0
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2
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3.8k
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Odds Ratio Confidence Intervals in SNP Test
Confidence-Interval OR CI SNPtest
updated 3.0 years ago by 45k • written 10.3 years ago by 4.8k
0
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0
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3.9k
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Comment: Comment: List of causal variants for autoimmune diseases
updated 2.9 years ago by 45k • written 10.3 years ago by 4.8k
0
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0
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2.2k
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How to find appropriate control regions for gene burden tests on T-cell enhancer regions
gene-burden enhancer control
10.4 years ago by LauferVA 4.8k
0
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0
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1.8k
views
Theoretical problems using PCA to control for cases and controls with different ethnicity
GWAS PCA
updated 2.9 years ago by 45k • written 10.4 years ago by 4.8k
0
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0
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2.1k
views
Most common method for looking at LD independent SNPs
Immunochip GWAS Bonferonni IChip LD
updated 2.9 years ago by 45k • written 10.4 years ago by 4.8k
0
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0
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1.6k
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Comment: Comment: Where to learn about getting a few thousand genomes sequenced?
updated 2.8 years ago by 45k • written 10.5 years ago by 4.8k
0
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2
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2.1k
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Genes with "AK#### or BC#####" in UCSC genome browser
UCSC gene track
updated 3.3 years ago by 45k • written 10.5 years ago by 4.8k
4
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2
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4.3k
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Using EPACTS to implement SKAT-O - question about ped files
SKAT EPACTS PED
updated 3.7 years ago by 45k • written 10.9 years ago by 4.8k
0
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0
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3.9k
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Comment: C: List of causal variants for autoimmune diseases
10.6 years ago by LauferVA 4.8k
0
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0
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3.9k
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Comment: Comment: List of causal variants for autoimmune diseases
updated 3.4 years ago by 45k • written 10.6 years ago by 4.8k
0
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0
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2.4k
views
Which HapMap Citation to cite if pulling information from dbSNP
MAF hapmap dbsnp
updated 3.4 years ago by 45k • written 10.6 years ago by 4.8k
1
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0
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3.9k
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Comment: Comment: Best implementation of negative binomial association test for GWAS data?
updated 3.6 years ago by 45k • written 10.8 years ago by 4.8k
9
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1
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6.4k
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Rationale for including a certain number of PCs in a GWAS study?
PCA Statistics GWAS
updated 10.8 years ago by ★ 4.8k • written 10.8 years ago by 4.8k
6
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1
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4.6k
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Answer: Answer: GWAS: low explained heritability
3.5 years ago by LauferVA 4.8k
1
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0
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4.8k
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Comment: Comment: how can I get MAF stratified by subpopulation for ASW, or CEU and YRI
updated 3.6 years ago by 45k • written 10.8 years ago by 4.8k
0
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1
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4.8k
views
Comment: Comment: how can I get MAF stratified by subpopulation for ASW, or CEU and YRI
updated 3.6 years ago by 45k • written 10.8 years ago by 4.8k
0
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1
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2.4k
views
Getting colors when displaying .bed files in locuszoom1.3
bed locuszoom graph
updated 3.6 years ago by 45k • written 10.8 years ago by 4.8k
2
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2
replies
3.3k
views
Bonferonni Correction for mostly overlapping enhancers
statistics bonferonni enhancers
updated 3.7 years ago by 45k • written 10.9 years ago by 4.8k
0
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0
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3.3k
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Comment: Comment: Bonferonni Correction for mostly overlapping enhancers
updated 3.7 years ago by 45k • written 10.9 years ago by 4.8k
6
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2
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2.9k
views
Options for generation of publication quality gene diagrams with annotation
VCF NGS Gene-Annotation
updated 3.8 years ago by 45k • written 11.1 years ago by 4.8k
793 results • Page 16 of 16
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