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Comment: C: Imputing specific SNPs using Beagle5.1
4.2 years ago by Vivek ★ 2.7k
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22k
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Comment: C: How Did You Learn Good Practice In Bioinformatics/Computational Biology?
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 2.7k
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8.0k
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Comment: C: GATK-Depth of Coverage - Issue with per gene coverage
updated 4.3 years ago by 43k • written 10.0 years ago by ★ 2.7k
3
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2
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6.3k
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Comment: C: How to interpret and extract from a Vcf file Genotype informations as values
updated 4.5 years ago by 43k • written 9.9 years ago by ★ 2.7k
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1
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1.8k
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Comment: C: Position error using write.plink
5.4 years ago by Vivek ★ 2.7k
1
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0
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2.3k
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Comment: C: GWAS data analysis strategy or pipeline
5.4 years ago by Vivek ★ 2.7k
1
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1
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2.3k
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Comment: C: GWAS data analysis strategy or pipeline
5.4 years ago by Vivek ★ 2.7k
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0
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1.4k
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Comment: C: Longitudinal Health Record Database Structure
5.5 years ago by Vivek ★ 2.7k
1
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0
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1.4k
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Comment: C: vcf file processing
5.9 years ago by Vivek ★ 2.7k
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1
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1.4k
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Comment: C: vcf file processing
5.9 years ago by Vivek ★ 2.7k
1
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1
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3.9k
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Comment: C: retrieving from ExAC in VCF format
6.7 years ago by Vivek ★ 2.7k
2
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1
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3.9k
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Comment: C: retrieving from ExAC in VCF format
6.7 years ago by Vivek ★ 2.7k
1
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1
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102k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.7 years ago by Vivek ★ 2.7k
2
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1
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102k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.7 years ago by Vivek ★ 2.7k
1
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3
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102k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.8 years ago by Vivek ★ 2.7k
1
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1
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102k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.8 years ago by Vivek ★ 2.7k
0
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1
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102k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.8 years ago by Vivek ★ 2.7k
0
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1
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102k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.8 years ago by Vivek ★ 2.7k
0
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1
reply
102k
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Comment: C: How to plot coverage and depth statistics of a bam file
6.8 years ago by Vivek ★ 2.7k
0
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0
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2.1k
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Comment: C: tips for checking variants in IGV
6.9 years ago by Vivek ★ 2.7k
0
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1
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4.8k
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Comment: C: how to analyse gene expression using RNA-seq data
7.2 years ago by Vivek ★ 2.7k
1
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1
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1.6k
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Comment: C: Mapping two WGS Data
7.3 years ago by Vivek ★ 2.7k
0
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1
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1.9k
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Comment: C: missing the variant NM_000251.2(MSH2):c.942+3A>T in variant calling
7.3 years ago by Vivek ★ 2.7k
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1
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1.5k
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Comment: C: identifying mutation & copy numbers using sequencing data
7.4 years ago by Vivek ★ 2.7k
0
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1
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3.1k
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Comment: C: Non-Bioinformatics Jobs with a Bioinformatics Degree
7.5 years ago by Vivek ★ 2.7k
1
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1
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3.5k
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Comment: C: Why is this insertion detected by NGS a false positive ?
7.5 years ago by Vivek ★ 2.7k
0
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1
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2.8k
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Comment: C: Method to merge two vcf files that don't have same alt information
7.7 years ago by Vivek ★ 2.7k
0
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0
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19k
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Comment: C: extract and generate a VCF file with only "PASS"
7.7 years ago by Vivek ★ 2.7k
0
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0
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7.1k
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Comment: C: CNVnator CNV-calling result interpretation
7.9 years ago by Vivek ★ 2.7k
0
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1
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7.1k
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Comment: C: CNVnator CNV-calling result interpretation
7.9 years ago by Vivek ★ 2.7k
0
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1
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3.1k
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Comment: C: Error in identification of genomic variants from RNA-seq.
7.9 years ago by Vivek ★ 2.7k
0
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2
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4.3k
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Comment: C: In RNA-seq data, how to find whether the mRNA is on the forward strand or revers
7.9 years ago by Vivek ★ 2.7k
0
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2
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3.7k
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Comment: C: vcf files in gatk not showing data lines
8.0 years ago by Vivek ★ 2.7k
0
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0
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6.3k
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Comment: C: How to interpret and extract from a Vcf file Genotype informations as values
8.0 years ago by Vivek ★ 2.7k
0
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1
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6.3k
views
Comment: C: How to interpret and extract from a Vcf file Genotype informations as values
8.0 years ago by Vivek ★ 2.7k
0
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1
reply
2.5k
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Comment: C: CNV detection by CopywriteR (bio conductor package )
8.1 years ago by Vivek ★ 2.7k
0
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1
reply
4.5k
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Comment: C: Do I need to use hg19 or hg38 reference for performing variant calling analysis
8.1 years ago by Vivek ★ 2.7k
0
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1
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8.3k
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Comment: C: UCSC hg19 gtf (genePredToGtf OS incompatibility)
8.2 years ago by Vivek ★ 2.7k
0
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0
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8.3k
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Comment: C: UCSC hg19 gtf (genePredToGtf OS incompatibility)
8.2 years ago by Vivek ★ 2.7k
1
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1
reply
66k
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Comment: C: VCF files: Change Chromosome Notation
8.2 years ago by Vivek ★ 2.7k
0
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0
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1.8k
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Comment: C: How can I serve a directory of BAM files via http most easily?
8.4 years ago by Vivek ★ 2.7k
0
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1
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2.1k
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Comment: C: Multiple Exon Start and End sites in UCSC Exons table
8.5 years ago by Vivek ★ 2.7k
0
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1
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5.2k
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Comment: C: Authorship issues- how to resolve?
8.9 years ago by Vivek ★ 2.7k
0
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1
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4.1k
views
Comment: Comment: Phasing trios for identification of denovo variants
updated 14 months ago by 43k • written 8.9 years ago by ★ 2.7k
0
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1
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2.1k
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Comment: Comment: Semantic verification of variants
updated 21 months ago by 43k • written 9.0 years ago by ★ 2.7k
0
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0
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7.7k
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Comment: A: Programatically retrieving CLINVAR records, with the same detail level as it is
9.0 years ago by Vivek ★ 2.7k
3
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0
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2.8k
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Comment: Comment: assign each SNP a strand information
updated 23 months ago by 43k • written 9.1 years ago by ★ 2.7k
0
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1
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2.8k
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Comment: C: assign each SNP a strand information
9.1 years ago by Vivek ★ 2.7k
0
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1
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3.0k
views
Comment: Comment: Reducing sequencing errors in .vcf file
updated 24 months ago by 43k • written 9.2 years ago by ★ 2.7k
0
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0
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1.9k
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Comment: Comment: Low quality reads causing false heterozygosity in SNP calling?
updated 2.1 years ago by 43k • written 9.3 years ago by ★ 2.7k
118 results • Page 1 of 3
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