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Comment: C: Imputing specific SNPs using Beagle5.1
3.6 years ago by Vivek ★ 2.7k
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21k
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Comment: C: How Did You Learn Good Practice In Bioinformatics/Computational Biology?
updated 3.7 years ago by 40k • written 9.4 years ago by ★ 2.7k
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7.8k
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Comment: C: GATK-Depth of Coverage - Issue with per gene coverage
updated 3.8 years ago by 40k • written 9.4 years ago by ★ 2.7k
3
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2
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5.8k
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Comment: C: How to interpret and extract from a Vcf file Genotype informations as values
updated 4.0 years ago by 40k • written 9.4 years ago by ★ 2.7k
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1
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1.6k
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Comment: C: Position error using write.plink
4.9 years ago by Vivek ★ 2.7k
1
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0
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2.1k
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Comment: C: GWAS data analysis strategy or pipeline
4.9 years ago by Vivek ★ 2.7k
1
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1
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2.1k
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Comment: C: GWAS data analysis strategy or pipeline
4.9 years ago by Vivek ★ 2.7k
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0
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1.3k
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Comment: C: Longitudinal Health Record Database Structure
5.0 years ago by Vivek ★ 2.7k
1
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0
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1.3k
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Comment: C: vcf file processing
5.3 years ago by Vivek ★ 2.7k
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1
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1.3k
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Comment: C: vcf file processing
5.3 years ago by Vivek ★ 2.7k
1
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1
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3.6k
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Comment: C: retrieving from ExAC in VCF format
6.2 years ago by Vivek ★ 2.7k
2
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1
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3.6k
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Comment: C: retrieving from ExAC in VCF format
6.2 years ago by Vivek ★ 2.7k
1
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1
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95k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.2 years ago by Vivek ★ 2.7k
2
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1
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95k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.2 years ago by Vivek ★ 2.7k
1
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3
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95k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.2 years ago by Vivek ★ 2.7k
1
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1
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95k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.2 years ago by Vivek ★ 2.7k
0
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1
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95k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.2 years ago by Vivek ★ 2.7k
0
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1
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95k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.3 years ago by Vivek ★ 2.7k
0
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1
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95k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.3 years ago by Vivek ★ 2.7k
0
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0
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1.9k
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Comment: C: tips for checking variants in IGV
6.3 years ago by Vivek ★ 2.7k
0
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1
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4.6k
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Comment: C: how to analyse gene expression using RNA-seq data
6.7 years ago by Vivek ★ 2.7k
1
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1
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1.5k
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Comment: C: Mapping two WGS Data
6.7 years ago by Vivek ★ 2.7k
0
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1
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1.7k
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Comment: C: missing the variant NM_000251.2(MSH2):c.942+3A>T in variant calling
6.8 years ago by Vivek ★ 2.7k
0
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1
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1.4k
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Comment: C: identifying mutation & copy numbers using sequencing data
6.8 years ago by Vivek ★ 2.7k
0
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1
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2.8k
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Comment: C: Non-Bioinformatics Jobs with a Bioinformatics Degree
6.9 years ago by Vivek ★ 2.7k
1
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1
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3.3k
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Comment: C: Why is this insertion detected by NGS a false positive ?
7.0 years ago by Vivek ★ 2.7k
0
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1
reply
2.6k
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Comment: C: Method to merge two vcf files that don't have same alt information
7.1 years ago by Vivek ★ 2.7k
0
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0
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17k
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Comment: C: extract and generate a VCF file with only "PASS"
7.1 years ago by Vivek ★ 2.7k
0
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0
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6.9k
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Comment: C: CNVnator CNV-calling result interpretation
7.3 years ago by Vivek ★ 2.7k
0
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1
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6.9k
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Comment: C: CNVnator CNV-calling result interpretation
7.3 years ago by Vivek ★ 2.7k
0
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1
reply
2.8k
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Comment: C: Error in identification of genomic variants from RNA-seq.
7.4 years ago by Vivek ★ 2.7k
0
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2
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4.0k
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Comment: C: In RNA-seq data, how to find whether the mRNA is on the forward strand or revers
7.4 years ago by Vivek ★ 2.7k
0
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2
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3.4k
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Comment: C: vcf files in gatk not showing data lines
7.5 years ago by Vivek ★ 2.7k
0
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0
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5.8k
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Comment: C: How to interpret and extract from a Vcf file Genotype informations as values
7.5 years ago by Vivek ★ 2.7k
0
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1
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5.8k
views
Comment: C: How to interpret and extract from a Vcf file Genotype informations as values
7.5 years ago by Vivek ★ 2.7k
0
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1
reply
2.4k
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Comment: C: CNV detection by CopywriteR (bio conductor package )
7.5 years ago by Vivek ★ 2.7k
0
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1
reply
4.2k
views
Comment: C: Do I need to use hg19 or hg38 reference for performing variant calling analysis
7.5 years ago by Vivek ★ 2.7k
0
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1
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7.8k
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Comment: C: UCSC hg19 gtf (genePredToGtf OS incompatibility)
7.6 years ago by Vivek ★ 2.7k
0
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0
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7.8k
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Comment: C: UCSC hg19 gtf (genePredToGtf OS incompatibility)
7.6 years ago by Vivek ★ 2.7k
1
vote
1
reply
59k
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Comment: C: VCF files: Change Chromosome Notation
7.6 years ago by Vivek ★ 2.7k
0
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0
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1.7k
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Comment: C: How can I serve a directory of BAM files via http most easily?
7.8 years ago by Vivek ★ 2.7k
0
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1
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2.0k
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Comment: C: Multiple Exon Start and End sites in UCSC Exons table
7.9 years ago by Vivek ★ 2.7k
0
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1
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4.4k
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Comment: C: Authorship issues- how to resolve?
8.3 years ago by Vivek ★ 2.7k
0
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1
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3.9k
views
Comment: Comment: Phasing trios for identification of denovo variants
updated 8 months ago by 40k • written 8.4 years ago by ★ 2.7k
0
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1
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1.9k
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Comment: Comment: Semantic verification of variants
updated 14 months ago by 40k • written 8.4 years ago by ★ 2.7k
0
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0
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7.1k
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Comment: A: Programatically retrieving CLINVAR records, with the same detail level as it is
8.5 years ago by Vivek ★ 2.7k
3
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0
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2.6k
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Comment: Comment: assign each SNP a strand information
updated 16 months ago by 40k • written 8.5 years ago by ★ 2.7k
0
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1
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2.6k
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Comment: C: assign each SNP a strand information
8.5 years ago by Vivek ★ 2.7k
0
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1
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2.7k
views
Comment: Comment: Reducing sequencing errors in .vcf file
updated 17 months ago by 40k • written 8.6 years ago by ★ 2.7k
0
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0
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1.8k
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Comment: Comment: Low quality reads causing false heterozygosity in SNP calling?
updated 18 months ago by 40k • written 8.8 years ago by ★ 2.7k
118 results • Page 1 of 3
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