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Converting GP field in a VCF to GT
VCF Threshold GT GP
2.4 years ago by Garan ▴ 690
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Answer: Answer: Converting GP field in a VCF to GT
2.4 years ago by Garan ▴ 690
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2.3k
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Answer: A: ICD10, main ICD10 and secondary ICD10
4.1 years ago by Garan ▴ 690
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1.6k
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Answer: A: Best way for CNV phenotype association analysis.
4.8 years ago by Garan ▴ 690
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3.2k
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Answer: A: ExomeDepth failure to run
5.0 years ago by Garan ▴ 690
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1.6k
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Comment: C: tools for MLST analysis
5.0 years ago by Garan ▴ 690
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1.1k
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Comment: C: Associate SNPs with Clinical Data
5.2 years ago by Garan ▴ 690
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Comment: C: how to perform GWAS on UKBiobank data?
5.4 years ago by Garan ▴ 690
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2.8k
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Comment: C: structural variants in gnomad and the VCF spec. Why is tabix/bcftools failing ?
5.4 years ago by Garan ▴ 690
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Answer: A: Gold standard CNV Calls for NA12878
5.5 years ago by Garan ▴ 690
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Comment: C: How can I do in GTAK downstream analysis?
5.6 years ago by Garan ▴ 690
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Answer: A: How can I do in GTAK downstream analysis?
5.6 years ago by Garan ▴ 690
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Answer: A: gnomAD: query utilitites
5.6 years ago by Garan ▴ 690
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3.5k
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Comment: C: Storing Varaint data from VCF
5.7 years ago by Garan ▴ 690
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3.5k
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Answer: A: Storing Varaint data from VCF
5.7 years ago by Garan ▴ 690
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2.4k
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Answer: A: Anyone know of a useful pedigree drawing program?
5.9 years ago by Garan ▴ 690
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2.2k
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Answer: A: Germline CNV Databases for Healthy and/or Cancer Patients
6.0 years ago by Garan ▴ 690
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2.0k
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Answer: A: how to identify disease variants from bam file ?
6.0 years ago by Garan ▴ 690
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3.7k
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Comment: C: CNV analysis from vcf file
6.1 years ago by Garan ▴ 690
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Comment: C: Most important International Big Data Projects: Genetics and Epigenetics
6.2 years ago by Garan ▴ 690
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3.3k
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Answer: A: NA12878 vs RM 8398 Reference DNA
6.2 years ago by Garan ▴ 690
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2.9k
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Comment: C: Visualizing body organs in R
6.2 years ago by Garan ▴ 690
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2.4k
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Answer: A: Identifying Split-Reads in WES data!
updated 6.2 years ago by 44k • written 8.8 years ago by ▴ 690
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Comment: C: Paternity Testing from WGS Trio
6.2 years ago by Garan ▴ 690
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2.8k
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Comment: C: Down sampling BAM files for CNV detection
6.3 years ago by Garan ▴ 690
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Comment: C: Down sampling BAM files for CNV detection
6.3 years ago by Garan ▴ 690
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2.8k
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Comment: C: Down sampling BAM files for CNV detection
6.3 years ago by Garan ▴ 690
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Answer: A: HLA Typing understanding
6.3 years ago by Garan ▴ 690
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Answer: A: How to select an aligner?
6.5 years ago by Garan ▴ 690
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5.0k
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Answer: A: Recommendations for CNV calling algorithms/programs to benchmark
6.8 years ago by Garan ▴ 690
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3.4k
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Answer: A: how to distinguish mosaicism out of germline de novo mutations
6.8 years ago by Garan ▴ 690
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2.3k
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Comment: C: FFPE samples for NGS
6.8 years ago by Garan ▴ 690
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3.4k
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Comment: C: Python Code to standardize gene name in CSV file
7.5 years ago by Garan ▴ 690
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3.3k
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Comment: C: Dealing with adjacent SNPs in VCF file
7.6 years ago by Garan ▴ 690
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3.1k
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Answer: A: Bioinformatics in a clinical diagnostic setting versus research (academia)
7.9 years ago by Garan ▴ 690
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2.5k
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Answer: A: functional assessment of synonymous SNPs
8.5 years ago by Garan ▴ 690
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2.0k
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Answer: A: website for clinical interpretation of NGS data
8.5 years ago by Garan ▴ 690
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7.0k
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Answer: A: How to detect CNV with panel sequencing?
8.7 years ago by Garan ▴ 690
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3.7k
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Answer: A: Bioinformatics for a medical student with interest in genetics
8.7 years ago by Garan ▴ 690
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1.8k
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Answer: Answer: Regarding Human Exon Variant Reference
updated 2.4 years ago by 44k • written 8.8 years ago by ▴ 690
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Answer: Answer: I would like to know how many synonimous mutations affect alternative spicing in
updated 2.2 years ago by 44k • written 9.2 years ago by ▴ 690
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Comment: Comment: websites about finding genes assiociated with rare-disease which is unreported b
updated 2.1 years ago by 44k • written 9.3 years ago by ▴ 690
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3.9k
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Answer: A: Bacterial identification - PCR primers - unknown target
9.6 years ago by Garan ▴ 690
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4.1k
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Answer: A: Bio-informatics for medical laboratory technologists
9.7 years ago by Garan ▴ 690
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6.7k
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Answer: Answer: Bioinformatic jobs outside academia?
updated 2.7 years ago by 44k • written 9.9 years ago by ▴ 690
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5.2k
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Answer: Answer: Can anyone with clinical experience tell me how to get involved in medical infor
updated 2.7 years ago by 44k • written 10.0 years ago by ▴ 690
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Answer: Answer: Filterout biallelic SNPs from multiple VCF files.
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 690
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Answer: A: Copy number variation detection tools within exome sequencing
10.0 years ago by Garan ▴ 690
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Answer: Answer: Identify gene symbols given a list of chromosome positions
updated 2.8 years ago by 44k • written 10.0 years ago by ▴ 690
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4.0k
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Answer: Answer: about the previous version of GATK
updated 2.9 years ago by 44k • written 10.2 years ago by ▴ 690
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