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2
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Comment: C: Interpreting the output of edgeR table coefficients
4.7 years ago by brunobsouzaa ▴ 840
1
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1
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818
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Comment: C: Differentially expressed genes selection by several pipelines
4.7 years ago by brunobsouzaa ▴ 840
1
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962
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Comment: C: Deviation from Hardy Weinberg equilibrium
4.7 years ago by brunobsouzaa ▴ 840
2
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1
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4.3k
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Comment: C: issues installing pathfindR package
4.8 years ago by brunobsouzaa ▴ 840
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0
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30k
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Comment: C: Gene Set Enrichment Analysis
4.8 years ago by brunobsouzaa ▴ 840
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1
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30k
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Comment: C: Gene Set Enrichment Analysis
updated 4.8 years ago by 45k • written 4.8 years ago by ▴ 840
0
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836
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Comment: C: Linkage disequilibrium program
4.8 years ago by brunobsouzaa ▴ 840
1
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0
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6.6k
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Comment: C: Error: Can't subset columns that don't exist. x Column `PEP` doesn't exist.
4.8 years ago by brunobsouzaa ▴ 840
2
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1
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6.6k
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Comment: A: Error: Can't subset columns that don't exist. x Column `PEP` doesn't exist.
4.8 years ago by brunobsouzaa ▴ 840
0
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0
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6.9k
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Comment: C: Error in GSEA function of clusterProfiler on R
4.8 years ago by brunobsouzaa ▴ 840
1
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2
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6.7k
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Comment: C: Is trimming necessary for RNAseq?
4.8 years ago by brunobsouzaa ▴ 840
1
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1
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923
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Comment: C: Calling CNVs from SNPs within targeted gene panel
4.8 years ago by brunobsouzaa ▴ 840
0
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0
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2.4k
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Comment: C: does RSEM need STAR?
4.8 years ago by brunobsouzaa ▴ 840
1
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2
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5.4k
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Comment: C: Why is gnomAD AF vs gnomAD exome AF so different?
4.8 years ago by brunobsouzaa ▴ 840
0
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1
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5.4k
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Comment: C: Why is gnomAD AF vs gnomAD exome AF so different?
4.8 years ago by brunobsouzaa ▴ 840
2
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1
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6.1k
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Answer: C: Convert CSV to PED
4.9 years ago by brunobsouzaa ▴ 840
1
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0
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1.3k
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Comment: C: Annotating variants using latest version fof the genome
4.9 years ago by brunobsouzaa ▴ 840
0
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1
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1.3k
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Answer: C: Annotating variants using latest version fof the genome
4.9 years ago by brunobsouzaa ▴ 840
1
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0
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1.7k
views
Comment: C: problem with a for loop
4.9 years ago by brunobsouzaa ▴ 840
1
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1
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1.7k
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Comment: C: problem with a for loop
4.9 years ago by brunobsouzaa ▴ 840
0
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0
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1.1k
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Comment: C: How to keep the input bed coordinates of a bed?
4.9 years ago by brunobsouzaa ▴ 840
1
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0
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2.8k
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Comment: C: merging vcf by vcftools
4.9 years ago by brunobsouzaa ▴ 840
0
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0
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3.3k
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Comment: C: How to Identify the pathogenicity of a set of variants (by using ACMG guidelines
4.9 years ago by brunobsouzaa ▴ 840
0
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1
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2.6k
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Comment: C: Plot GWAS p value distribution for multiple traits
4.9 years ago by brunobsouzaa ▴ 840
0
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1
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3.5k
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Comment: C: Exception in thread "main" java.lang.RuntimeException: Unknown trimmer
4.9 years ago by brunobsouzaa ▴ 840
2
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1
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3.5k
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Comment: C: Exception in thread "main" java.lang.RuntimeException: Unknown trimmer
4.9 years ago by brunobsouzaa ▴ 840
0
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0
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2.1k
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Comment: C: Count SNPs using bcftools
4.9 years ago by brunobsouzaa ▴ 840
0
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1
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2.1k
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Comment: C: Count SNPs using bcftools
4.9 years ago by brunobsouzaa ▴ 840
0
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0
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1.4k
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Comment: C: Differencial expression analysis between groups determined by two variables
4.9 years ago by brunobsouzaa ▴ 840
0
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1
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2.1k
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Comment: C: Count SNPs using bcftools
4.9 years ago by brunobsouzaa ▴ 840
0
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0
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1.4k
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Comment: C: CNVkit germline CNV calling error.
4.9 years ago by brunobsouzaa ▴ 840
0
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1
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2.1k
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Comment: C: Count SNPs using bcftools
5.0 years ago by brunobsouzaa ▴ 840
0
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1
reply
2.1k
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Comment: C: Count SNPs using bcftools
5.0 years ago by brunobsouzaa ▴ 840
1
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0
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3.2k
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Comment: C: E: Package 'tophat' has no installation candidate
5.0 years ago by brunobsouzaa ▴ 840
0
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0
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3.4k
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Comment: C: STAR-fusion: preparing the human genome resource lib
5.0 years ago by brunobsouzaa ▴ 840
0
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0
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3.4k
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Comment: C: STAR-fusion: preparing the human genome resource lib
5.0 years ago by brunobsouzaa ▴ 840
0
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0
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998
views
Comment: C: annovar continues to use hg18 version despite using buildver hg19 argument
5.0 years ago by brunobsouzaa ▴ 840
0
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1
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1.4k
views
Comment: C: validation copy number variations in whole genomes
5.0 years ago by brunobsouzaa ▴ 840
0
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1
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1.4k
views
Comment: C: validation copy number variations in whole genomes
5.0 years ago by brunobsouzaa ▴ 840
0
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1
reply
1.4k
views
Comment: C: validation copy number variations in whole genomes
5.0 years ago by brunobsouzaa ▴ 840
0
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1
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999
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Comment: C: variant identification ngs
5.0 years ago by brunobsouzaa ▴ 840
0
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1
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1.8k
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Comment: C: Merging BAM or VCF files, whats the difference?
5.0 years ago by brunobsouzaa ▴ 840
5
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1
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2.1k
views
Answer: A: Finding unique variants by sample ID in a multisample vcf
5.0 years ago by brunobsouzaa ▴ 840
1
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1
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1.9k
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Comment: C: plink case/control association analysis and Manhattan plot
5.0 years ago by brunobsouzaa ▴ 840
0
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0
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1.3k
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Comment: C: Test for genetic additive model using R
5.0 years ago by brunobsouzaa ▴ 840
2
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2
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1.3k
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Test for genetic additive model using R
Additive SNP R
5.0 years ago by brunobsouzaa ▴ 840
1
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1
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2.5k
views
Comment: C: Best way to get Allele Frequency in dbSNP file of SNPs in a different VCF file?
5.0 years ago by brunobsouzaa ▴ 840
0
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0
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1.3k
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Comment: C: Calling CNVs using a single tumor sample
5.0 years ago by brunobsouzaa ▴ 840
0
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0
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3.6k
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Comment: C: RNASeq data: STAR low alignment score
5.0 years ago by brunobsouzaa ▴ 840
0
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1
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1.7k
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Comment: C: Visual summary from a collection of .vcf files (WES)
5.1 years ago by brunobsouzaa ▴ 840
212 results • Page 3 of 5
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