Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
1
vote
1
reply
709
views
Comment: C: Calling CNVs from SNPs within targeted gene panel
3.5 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
1.9k
views
Comment: C: does RSEM need STAR?
3.5 years ago by brunobsouzaa ▴ 830
1
vote
2
replies
3.5k
views
Comment: C: Why is gnomAD AF vs gnomAD exome AF so different?
3.5 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
3.5k
views
Comment: C: Why is gnomAD AF vs gnomAD exome AF so different?
3.5 years ago by brunobsouzaa ▴ 830
1
vote
0
replies
854
views
Comment: C: Annotating variants using latest version fof the genome
3.6 years ago by brunobsouzaa ▴ 830
1
vote
0
replies
1.2k
views
Comment: C: problem with a for loop
3.6 years ago by brunobsouzaa ▴ 830
1
vote
1
reply
1.2k
views
Comment: C: problem with a for loop
3.6 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
846
views
Comment: C: How to keep the input bed coordinates of a bed?
3.6 years ago by brunobsouzaa ▴ 830
1
vote
0
replies
2.5k
views
Comment: C: merging vcf by vcftools
3.6 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.2k
views
Comment: C: How to Identify the pathogenicity of a set of variants (by using ACMG guidelines
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.9k
views
Comment: C: Plot GWAS p value distribution for multiple traits
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
2.6k
views
Comment: C: Exception in thread "main" java.lang.RuntimeException: Unknown trimmer
3.6 years ago by brunobsouzaa ▴ 830
2
votes
1
reply
2.6k
views
Comment: C: Exception in thread "main" java.lang.RuntimeException: Unknown trimmer
3.6 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
1.6k
views
Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.6k
views
Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
1.0k
views
Comment: C: Differencial expression analysis between groups determined by two variables
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.6k
views
Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
1.1k
views
Comment: C: CNVkit germline CNV calling error.
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.6k
views
Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.6k
views
Comment: C: Count SNPs using bcftools
3.6 years ago by brunobsouzaa ▴ 830
1
vote
0
replies
2.6k
views
Comment: C: E: Package 'tophat' has no installation candidate
3.6 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.7k
views
Comment: C: STAR-fusion: preparing the human genome resource lib
3.6 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.7k
views
Comment: C: STAR-fusion: preparing the human genome resource lib
3.6 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
698
views
Comment: C: annovar continues to use hg18 version despite using buildver hg19 argument
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
923
views
Comment: C: validation copy number variations in whole genomes
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
923
views
Comment: C: validation copy number variations in whole genomes
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
923
views
Comment: C: validation copy number variations in whole genomes
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
695
views
Comment: C: variant identification ngs
3.6 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.4k
views
Comment: C: Merging BAM or VCF files, whats the difference?
3.6 years ago by brunobsouzaa ▴ 830
1
vote
1
reply
1.5k
views
Comment: C: plink case/control association analysis and Manhattan plot
3.7 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
945
views
Comment: C: Test for genetic additive model using R
3.7 years ago by brunobsouzaa ▴ 830
1
vote
1
reply
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
votes
0
replies
1000
views
Comment: C: Calling CNVs using a single tumor sample
3.7 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.7k
views
Comment: C: RNASeq data: STAR low alignment score
3.7 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.3k
views
Comment: C: Visual summary from a collection of .vcf files (WES)
3.7 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.7k
views
Comment: C: RNASeq data: STAR low alignment score
3.7 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.6k
views
Comment: C: Merging BAM vs concatenate FASTQ
3.7 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
12k
views
Comment: Comment: How to count SNPs, InDels
updated 18 months ago by 43k • written 3.7 years ago by ▴ 830
0
votes
1
reply
819
views
Comment: C: Generate .bed file with exon and intron indices
3.8 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
928
views
Comment: C: online link for SNP genotype frequency calculations
3.8 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
11k
views
Comment: C: Run Fastqc from terminal
3.8 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
2.0k
views
Comment: C: Database for germline mutations
3.8 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.0k
views
Comment: C: Database for germline mutations
3.8 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
1.1k
views
Comment: C: GATK variant calling
3.8 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.1k
views
Comment: C: GATK variant calling
3.8 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
4.4k
views
Comment: C: How to analyze Illumina RNASeq data
3.8 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.7k
views
Comment: C: How to download seqret method in Linux?
3.8 years ago by brunobsouzaa ▴ 830
0
votes
0
replies
2.5k
views
Comment: C: Noisy germline CNV data using CNVKit
3.8 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
1.1k
views
Comment: C: How to annotate variants offline using ANNOVAR?
3.8 years ago by brunobsouzaa ▴ 830
0
votes
1
reply
6.2k
views
Comment: C: ACMG assignment tools
3.8 years ago by brunobsouzaa ▴ 830
174 results • Page 3 of 4
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6