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4.6k
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Answer: A: how to analyse gene expression using RNA-seq data
6.7 years ago by Vivek ★ 2.7k
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1
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1.8k
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Answer: A: SVM based Filtering For NGS data
6.7 years ago by Vivek ★ 2.7k
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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
1
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2
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1.5k
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Answer: A: Mapping two WGS Data
6.7 years ago by Vivek ★ 2.7k
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0
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2.6k
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Answer: A: Annovar Output column "AAChange.knowngene" gives different values
6.7 years ago by Vivek ★ 2.7k
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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
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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
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1
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1.4k
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Answer: A: identifying mutation & copy numbers using sequencing data
6.8 years ago by Vivek ★ 2.7k
1
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0
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1.6k
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Answer: A: Software to identify and classify disease-relevant variants
6.9 years ago by Vivek ★ 2.7k
7
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1
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2.6k
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Answer: A: Is it better to remove MT reads by removing the MT Chromosome from your fasta or
6.9 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
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1.4k
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Answer: A: Some tricks from the experts
6.9 years ago by Vivek ★ 2.7k
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0
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1.9k
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Adjusting for population substructure in heterozygosity using regression with PCs
GWAS QC PCA heterozygosity
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
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0
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1.1k
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shellfish hapmap PCA loadings
gwas shellfish pca snp loadings
updated 7.0 years ago by 134k • written 7.0 years ago by ★ 2.7k
16
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11
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8.6k
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Identifying De Novo Variants In Trio Data
variant gatk differential-expression
updated 20 months ago by 40k • written 11.2 years ago by ★ 2.7k
0
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0
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3.0k
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Answer: A: Bioinformatics tech vs Bioinformatics scientist
7.1 years ago by Vivek ★ 2.7k
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1
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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
2
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1
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2.6k
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Answer: A: Method to merge two vcf files that don't have same alt information
7.1 years ago by Vivek ★ 2.7k
5
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1
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17k
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Answer: A: 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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17k
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Comment: C: extract and generate a VCF file with only "PASS"
7.1 years ago by Vivek ★ 2.7k
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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
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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
3
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0
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8.5k
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Answer: A: Good Habit for Bioinformatics Analyst or Scientist
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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1
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2.6k
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Answer: A: How to merge different strain SNP vcf files into one combined vcf file with stra
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
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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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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
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4.2k
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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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0
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2.4k
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Answer: A: getting germline mutations
7.5 years ago by Vivek ★ 2.7k
4
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1
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4.2k
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Answer: A: 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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3.7k
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Answer: A: VCF to genotype file of specific format
7.6 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
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1
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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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2.8k
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Job: Bioinformatics Programmer at Baylor College of Medicine, Houston TX
bionformatician houston
updated 14 months ago by 40k • written 7.7 years ago by ★ 2.7k
3
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0
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3.4k
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Answer: A: How can I compare two columns of a two VCF files
7.7 years ago by Vivek ★ 2.7k
1
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0
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2.0k
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Answer: A: Discrepancy between Whole Exome Sequence result and Sanger Sequence result
7.7 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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2.4k
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Answer: A: two questions in loading data
7.9 years ago by Vivek ★ 2.7k
0
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0
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4.3k
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Answer: A: Hot research areas in Bioinformatics for career development
7.9 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
1
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0
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2.9k
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Answer: Answer: How to check the reads coverage of an area in ExAC, ESP6500, and 1000Genomes
updated 12 months ago by 40k • written 8.1 years ago by ★ 2.7k
0
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0
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2.0k
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Answer: Answer: What are the different ways of referring to a genetic variant/ mutation?
updated 12 months ago by 40k • written 8.1 years ago by ★ 2.7k
3
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1
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3.0k
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Answer: A: How to bulk convert coding position of transkript to genomic positions?
8.3 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
1
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0
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4.4k
views
Answer: Answer: Authorship issues- how to resolve?
updated 8 months ago by 40k • written 8.3 years ago by ★ 2.7k
232 results • Page 2 of 5
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