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Answer: Answer: Protein prediction tool
2.5 years ago by Collin ▴ 1000
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Answer: Answer: Can non-driver mutations disrupt the function of proteins and further affect a c
2.6 years ago by Collin ▴ 1000
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Answer: Answer: Identification of transcription factors from a list of DEGs
2.7 years ago by Collin ▴ 1000
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Answer: Answer: Association analysis with SNP
2.7 years ago by Collin ▴ 1000
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Answer: Answer: Preparing CHASMplus database for annotation
2.8 years ago by Collin ▴ 1000
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Answer: A: Is there a tool to predict if a missense variant causes a loss of function on th
updated 3.1 years ago by 141k • written 3.3 years ago by ▴ 1000
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Answer: Answer: SNP annotation tool
updated 2.2 years ago by 43k • written 3.4 years ago by ▴ 1000
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1.9k
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Answer: C: TCGA driver mutation data
3.5 years ago by Collin ▴ 1000
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4.0k
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Answer: C: Get clinVar info for SNP with VEP
3.9 years ago by Collin ▴ 1000
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1.2k
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Answer: A: How to download passenger mutations for cancer
4.1 years ago by Collin ▴ 1000
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Answer: A: Getting a list of tumor suppressors
4.1 years ago by Collin ▴ 1000
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3.9k
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Answer: A: Can't open file 'features': [Errno 2] No such file or directory
4.2 years ago by Collin ▴ 1000
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1.2k
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Answer: A: Cancer driver mutations Identification from VCFs
4.2 years ago by Collin ▴ 1000
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Answer: A: about snp prediction
4.2 years ago by Collin ▴ 1000
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1.2k
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Answer: A: Somatic Variant Annotation and Interpretation
4.2 years ago by Collin ▴ 1000
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4.5k
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Answer: A: Indel Annotation Tools, Not Loss Of Function
4.3 years ago by Collin ▴ 1000
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4.8k
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Answer: A: How to "merge" monomeric structures in COOT (WinCoot) - pdb files
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 1000
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2.5k
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Answer: A: Are there certain mutations ubiquitous in ALL cancers?
updated 4.4 years ago by 43k • written 8.4 years ago by ▴ 1000
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17k
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Answer: A: Benjamini+ Hochberg multiple testing p.adjust R
5.8 years ago by Collin ▴ 1000
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2.4k
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Answer: A: Constructing a mean ROC curve based on 5 iterations
5.8 years ago by Collin ▴ 1000
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1.2k
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Answer: A: Alternative tools replace MutDB to predict consequences of deleterious SNV
6.2 years ago by Collin ▴ 1000
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1.7k
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Answer: A: 2020+ installation problems:
6.4 years ago by Collin ▴ 1000
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1.6k
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Answer: A: Input file requirements for hg38
6.5 years ago by Collin ▴ 1000
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2.1k
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Answer: A: BRCA1 and BRCA2 database's for NGS diagnostics purposes
6.6 years ago by Collin ▴ 1000
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2.6k
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Answer: A: Statistical test for finding driver mutations.
7.0 years ago by Collin ▴ 1000
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3.7k
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Answer: A: How to conduct pathway analysis from VCF file?
7.2 years ago by Collin ▴ 1000
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Answer: C: Effect size of a SNP - contribution to genetic variance
7.4 years ago by Collin ▴ 1000
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Answer: A: User Friendly VCF Filtering Tools
7.9 years ago by Collin ▴ 1000
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11k
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Answer: Answer: Map genetic mutations to protein domain/structure
updated 2.1 years ago by 43k • written 7.9 years ago by ▴ 1000
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2.3k
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Answer: A: Difficulty replicating likelihood ratio test from RNA-seq paper
8.0 years ago by Collin ▴ 1000
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1.8k
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Answer: A: COSMIC data and rare variant
8.1 years ago by Collin ▴ 1000
2
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0
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14k
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Answer: Answer: Best Graphics Gallery Or Blogs For Bioinformatics Use
updated 20 months ago by 43k • written 8.3 years ago by ▴ 1000
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