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2
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3.2k
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Comment: C: Interpreting the output of edgeR table coefficients
3.4 years ago by brunobsouzaa ▴ 830
1
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1
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617
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Comment: C: Differentially expressed genes selection by several pipelines
3.4 years ago by brunobsouzaa ▴ 830
1
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0
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733
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Comment: C: Deviation from Hardy Weinberg equilibrium
3.4 years ago by brunobsouzaa ▴ 830
2
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1
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3.2k
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Comment: C: issues installing pathfindR package
3.4 years ago by brunobsouzaa ▴ 830
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0
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23k
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Comment: C: Gene Set Enrichment Analysis
3.4 years ago by brunobsouzaa ▴ 830
0
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1
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23k
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Comment: C: Gene Set Enrichment Analysis
updated 3.4 years ago by 43k • written 3.4 years ago by ▴ 830
0
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0
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662
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Comment: C: Linkage disequilibrium program
3.4 years ago by brunobsouzaa ▴ 830
1
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0
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5.5k
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Comment: C: Error: Can't subset columns that don't exist. x Column `PEP` doesn't exist.
3.4 years ago by brunobsouzaa ▴ 830
2
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1
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5.5k
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Comment: A: Error: Can't subset columns that don't exist. x Column `PEP` doesn't exist.
3.4 years ago by brunobsouzaa ▴ 830
0
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0
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5.0k
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Comment: C: Error in GSEA function of clusterProfiler on R
3.4 years ago by brunobsouzaa ▴ 830
1
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2
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4.5k
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Comment: C: Is trimming necessary for RNAseq?
3.5 years ago by brunobsouzaa ▴ 830
1
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1
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700
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Comment: C: Calling CNVs from SNPs within targeted gene panel
3.5 years ago by brunobsouzaa ▴ 830
0
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0
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1.9k
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Comment: C: does RSEM need STAR?
3.5 years ago by brunobsouzaa ▴ 830
1
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2
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3.5k
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Comment: C: Why is gnomAD AF vs gnomAD exome AF so different?
3.5 years ago by brunobsouzaa ▴ 830
0
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1
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3.5k
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Comment: C: Why is gnomAD AF vs gnomAD exome AF so different?
3.5 years ago by brunobsouzaa ▴ 830
2
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1
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4.4k
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Answer: C: Convert CSV to PED
3.5 years ago by brunobsouzaa ▴ 830
1
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0
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845
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Comment: C: Annotating variants using latest version fof the genome
3.5 years ago by brunobsouzaa ▴ 830
0
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1
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845
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Answer: C: Annotating variants using latest version fof the genome
3.5 years ago by brunobsouzaa ▴ 830
1
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0
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1.2k
views
Comment: C: problem with a for loop
3.6 years ago by brunobsouzaa ▴ 830
1
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1
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1.2k
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Comment: C: problem with a for loop
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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841
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Comment: C: How to keep the input bed coordinates of a bed?
3.6 years ago by brunobsouzaa ▴ 830
1
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0
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2.5k
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Comment: C: merging vcf by vcftools
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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2.2k
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Comment: C: How to Identify the pathogenicity of a set of variants (by using ACMG guidelines
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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1.9k
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Comment: C: Plot GWAS p value distribution for multiple traits
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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2.6k
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Comment: C: Exception in thread "main" java.lang.RuntimeException: Unknown trimmer
3.6 years ago by brunobsouzaa ▴ 830
2
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1
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2.6k
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Comment: C: Exception in thread "main" java.lang.RuntimeException: Unknown trimmer
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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1.6k
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Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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1.6k
views
Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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1.0k
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Comment: C: Differencial expression analysis between groups determined by two variables
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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1.6k
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Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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1.1k
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Comment: C: CNVkit germline CNV calling error.
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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1.6k
views
Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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1.6k
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Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
1
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0
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2.6k
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Comment: C: E: Package 'tophat' has no installation candidate
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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2.7k
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Comment: C: STAR-fusion: preparing the human genome resource lib
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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2.7k
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Comment: C: STAR-fusion: preparing the human genome resource lib
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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692
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Comment: C: annovar continues to use hg18 version despite using buildver hg19 argument
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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911
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Comment: C: validation copy number variations in whole genomes
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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911
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Comment: C: validation copy number variations in whole genomes
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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911
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Comment: C: validation copy number variations in whole genomes
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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687
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Comment: C: variant identification ngs
3.6 years ago by brunobsouzaa ▴ 830
0
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1
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1.4k
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Comment: C: Merging BAM or VCF files, whats the difference?
3.6 years ago by brunobsouzaa ▴ 830
5
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1
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1.6k
views
Answer: A: Finding unique variants by sample ID in a multisample vcf
3.6 years ago by brunobsouzaa ▴ 830
1
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1
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1.5k
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Comment: C: plink case/control association analysis and Manhattan plot
3.6 years ago by brunobsouzaa ▴ 830
0
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0
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942
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Comment: C: Test for genetic additive model using R
3.7 years ago by brunobsouzaa ▴ 830
2
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2
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942
views
Test for genetic additive model using R
Additive SNP R
3.7 years ago by brunobsouzaa ▴ 830
1
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1
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1.9k
views
Comment: C: Best way to get Allele Frequency in dbSNP file of SNPs in a different VCF file?
3.7 years ago by brunobsouzaa ▴ 830
0
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0
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995
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Comment: C: Calling CNVs using a single tumor sample
3.7 years ago by brunobsouzaa ▴ 830
0
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0
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2.7k
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Comment: C: RNASeq data: STAR low alignment score
3.7 years ago by brunobsouzaa ▴ 830
0
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1
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1.2k
views
Comment: C: Visual summary from a collection of .vcf files (WES)
3.7 years ago by brunobsouzaa ▴ 830
212 results • Page 3 of 5
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