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2
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191k
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Answer: Answer: How to download raw sequence data from GEO/SRA
6 weeks ago by geocarvalho ▴ 390
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0
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12k
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Answer: Answer: bedGraphToBigWig Install error
16 months ago by geocarvalho ▴ 390
1
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1
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4.2k
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Answer: Answer: How to run Picard docker image
18 months ago by geocarvalho ▴ 390
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8.6k
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Answer: Answer: filtering the reads based on the length
18 months ago by geocarvalho ▴ 390
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1.6k
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Answer: Answer: Removing multi-variant records from vcf file
19 months ago by geocarvalho ▴ 390
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1.2k
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Answer: Answer: GATK4 ASEReadCounter Function of VCF
19 months ago by geocarvalho ▴ 390
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0
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6.4k
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Answer: Answer: How to access specifically 30x NA12878 sequencing runs
8 months ago by geocarvalho ▴ 390
4
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0
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8.6k
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Answer: Answer: snpEFF not able to download GRCH38 ?
3.2 years ago by geocarvalho ▴ 390
1
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0
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25k
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Answer: A: Where to download blacklisted regions?
4.4 years ago by geocarvalho ▴ 390
1
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0
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2.3k
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Answer: A: CNV and pseudogenes
4.6 years ago by geocarvalho ▴ 390
9
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1
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94k
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Answer: A: Extract Sub-Set Of Regions From Vcf File
updated 5.0 years ago by 44k • written 7.2 years ago by ▴ 390
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2.5k
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Answer: A: Trying to Identify larger indels from NGS data, FASTQ format
5.6 years ago by geocarvalho ▴ 390
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1.7k
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Answer: A: Annotation tool for cnvKit
6.0 years ago by geocarvalho ▴ 390
0
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0
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1.9k
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Answer: A: Bioinformatics workshop or training courses
6.3 years ago by geocarvalho ▴ 390
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0
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1.5k
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Answer: A: Large deletions in exome sequencing data
6.5 years ago by geocarvalho ▴ 390
2
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1
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3.0k
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Answer: A: Identifying CNVs from targeted amplicon sequencing
6.5 years ago by geocarvalho ▴ 390
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0
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3.1k
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Answer: A: Plotting common SNPs from four individual from a vcf file
6.8 years ago by geocarvalho ▴ 390
2
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0
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2.8k
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Answer: A: R books with Quantitative Genetics examples?
6.8 years ago by geocarvalho ▴ 390
1
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0
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1.5k
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Answer: A: Packages/modules for CNV, Indels, SNPs analysis
6.8 years ago by geocarvalho ▴ 390
4
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0
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14k
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Answer: A: List all available databases for ANNOVAR
7.0 years ago by geocarvalho ▴ 390
2
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0
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4.3k
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Answer: A: vcfeval Error: No sample name provided but calls is a multi-sample VCF
7.0 years ago by geocarvalho ▴ 390
0
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1
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2.2k
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Answer: A: How to start analyzing next-generation DNA and RNA sequencing data?
7.1 years ago by geocarvalho ▴ 390
1
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0
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1.8k
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Answer: A: Where can I find a sample analysis pipeline for DNA?
7.6 years ago by geocarvalho ▴ 390
0
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1
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1.8k
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Answer: A: Different reference and variant allele in IonTorrent variantCaller
7.7 years ago by geocarvalho ▴ 390
1
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0
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5.1k
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Answer: A: Copy Number Variation Tools
7.7 years ago by geocarvalho ▴ 390
0
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0
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7.1k
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Answer: A: Annotation of Structural Variants and CNVs
7.8 years ago by geocarvalho ▴ 390
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