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Answer:
Answer: Converting GP field in a VCF to GT
22 months ago by
Garan
▴ 690
2
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0
replies
1.9k
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Answer:
A: ICD10, main ICD10 and secondary ICD10
3.5 years ago by
Garan
▴ 690
1
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1
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1.4k
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Answer:
A: Best way for CNV phenotype association analysis.
4.2 years ago by
Garan
▴ 690
2
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1
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2.9k
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Answer:
A: ExomeDepth failure to run
4.4 years ago by
Garan
▴ 690
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5.6k
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Answer:
A: Gold standard CNV Calls for NA12878
4.9 years ago by
Garan
▴ 690
2
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1
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1.7k
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Answer:
A: How can I do in GTAK downstream analysis?
5.0 years ago by
Garan
▴ 690
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4.6k
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Answer:
A: gnomAD: query utilitites
5.1 years ago by
Garan
▴ 690
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1
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3.2k
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Answer:
A: Storing Varaint data from VCF
5.2 years ago by
Garan
▴ 690
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2.3k
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Answer:
A: Anyone know of a useful pedigree drawing program?
5.4 years ago by
Garan
▴ 690
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2.0k
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Answer:
A: Germline CNV Databases for Healthy and/or Cancer Patients
5.4 years ago by
Garan
▴ 690
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1.9k
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Answer:
A: how to identify disease variants from bam file ?
5.5 years ago by
Garan
▴ 690
4
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3.2k
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Answer:
A: NA12878 vs RM 8398 Reference DNA
5.6 years ago by
Garan
▴ 690
1
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1
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2.2k
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Answer:
A: Identifying Split-Reads in WES data!
updated 5.6 years ago by
Ram
43k • written 8.2 years ago by
Garan
▴ 690
1
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0
replies
1.8k
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Answer:
A: HLA Typing understanding
5.7 years ago by
Garan
▴ 690
4
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1
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12k
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Answer:
A: How to select an aligner?
5.9 years ago by
Garan
▴ 690
10
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2
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4.7k
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Answer:
A: Recommendations for CNV calling algorithms/programs to benchmark
6.2 years ago by
Garan
▴ 690
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1
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3.2k
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Answer:
A: how to distinguish mosaicism out of germline de novo mutations
6.2 years ago by
Garan
▴ 690
1
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0
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2.9k
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Answer:
A: Bioinformatics in a clinical diagnostic setting versus research (academia)
7.3 years ago by
Garan
▴ 690
1
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0
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2.4k
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Answer:
A: functional assessment of synonymous SNPs
7.9 years ago by
Garan
▴ 690
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0
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1.8k
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Answer:
A: website for clinical interpretation of NGS data
8.0 years ago by
Garan
▴ 690
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6.8k
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Answer:
A: How to detect CNV with panel sequencing?
8.2 years ago by
Garan
▴ 690
4
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2
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3.4k
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Answer:
A: Bioinformatics for a medical student with interest in genetics
8.2 years ago by
Garan
▴ 690
1
vote
1
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1.7k
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Answer:
Answer: Regarding Human Exon Variant Reference
updated 21 months ago by
Ram
43k • written 8.2 years ago by
Garan
▴ 690
0
votes
0
replies
1.9k
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Answer:
Answer: I would like to know how many synonimous mutations affect alternative spicing in
updated 20 months ago by
Ram
43k • written 8.6 years ago by
Garan
▴ 690
3
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0
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3.8k
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Answer:
A: Bacterial identification - PCR primers - unknown target
9.0 years ago by
Garan
▴ 690
2
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0
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3.9k
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Answer:
A: Bio-informatics for medical laboratory technologists
9.1 years ago by
Garan
▴ 690
2
votes
0
replies
6.4k
views
Answer:
Answer: Bioinformatic jobs outside academia?
updated 2.1 years ago by
Ram
43k • written 9.3 years ago by
Garan
▴ 690
5
votes
1
reply
5.1k
views
Answer:
Answer: Can anyone with clinical experience tell me how to get involved in medical infor
updated 2.1 years ago by
Ram
43k • written 9.4 years ago by
Garan
▴ 690
2
votes
0
replies
6.4k
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Answer:
Answer: Filterout biallelic SNPs from multiple VCF files.
updated 2.2 years ago by
Ram
43k • written 9.5 years ago by
Garan
▴ 690
3
votes
0
replies
3.2k
views
Answer:
A: Copy number variation detection tools within exome sequencing
9.5 years ago by
Garan
▴ 690
1
vote
0
replies
15k
views
Answer:
Answer: Identify gene symbols given a list of chromosome positions
updated 2.2 years ago by
Ram
43k • written 9.5 years ago by
Garan
▴ 690
3
votes
2
replies
3.8k
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Answer:
Answer: about the previous version of GATK
updated 2.4 years ago by
Ram
43k • written 9.7 years ago by
Garan
▴ 690
1
vote
1
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19k
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Answer:
Answer: Crac: Funny And/Or Weird Names For Bioinformatics Tools
updated 2.3 years ago by
Ram
43k • written 9.6 years ago by
Garan
▴ 690
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