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Answer: Answer: Protein prediction tool
3.1 years ago by Collin ▴ 1000
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
3.2 years ago by Collin ▴ 1000
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1.6k
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
3.2 years ago by Collin ▴ 1000
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1.6k
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Answer: Answer: Can non-driver mutations disrupt the function of proteins and further affect a c
3.2 years ago by Collin ▴ 1000
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Answer: Answer: Identification of transcription factors from a list of DEGs
3.3 years ago by Collin ▴ 1000
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763
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Answer: Answer: Association analysis with SNP
3.4 years ago by Collin ▴ 1000
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Comment: Comment: Preparing CHASMplus database for annotation
3.4 years ago by Collin ▴ 1000
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1.6k
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Comment: Comment: Preparing CHASMplus database for annotation
3.4 years ago by Collin ▴ 1000
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1.6k
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Answer: Answer: Preparing CHASMplus database for annotation
3.4 years ago by Collin ▴ 1000
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5.4k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
3.4 years ago by Collin ▴ 1000
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5.4k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
3.5 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 3.7 years ago by 147k • written 3.9 years ago by ▴ 1000
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Comment: C: VEP is very slow. Fork doesnt seem to work
3.7 years ago by Collin ▴ 1000
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3.8k
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Comment: C: VEP is very slow. Fork doesnt seem to work
3.7 years ago by Collin ▴ 1000
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2.7k
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Comment: C: Is there a tool to predict if a missense variant causes a loss of function on th
3.9 years ago by Collin ▴ 1000
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26k
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Answer: Answer: SNP annotation tool
updated 2.8 years ago by 44k • written 4.0 years ago by ▴ 1000
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2.2k
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Comment: C: TCGA driver mutation data
4.1 years ago by Collin ▴ 1000
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1.7k
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Comment: C: Protein_Change in MAF
4.1 years ago by Collin ▴ 1000
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2.2k
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Comment: C: TCGA driver mutation data
4.1 years ago by Collin ▴ 1000
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2.2k
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Comment: C: TCGA driver mutation data
4.1 years ago by Collin ▴ 1000
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2.2k
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Comment: C: TCGA driver mutation data
4.1 years ago by Collin ▴ 1000
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2.2k
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Comment: C: TCGA driver mutation data
4.1 years ago by Collin ▴ 1000
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2.2k
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Answer: C: TCGA driver mutation data
4.1 years ago by Collin ▴ 1000
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1.3k
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
4.2 years ago by Collin ▴ 1000
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1.3k
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
4.2 years ago by Collin ▴ 1000
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4.8k
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Comment: C: Get clinVar info for SNP with VEP
4.5 years ago by Collin ▴ 1000
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4.8k
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Comment: C: Get clinVar info for SNP with VEP
4.5 years ago by Collin ▴ 1000
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4.8k
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Answer: C: Get clinVar info for SNP with VEP
4.5 years ago by Collin ▴ 1000
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1.1k
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Comment: C: Variant effect prediction
4.6 years ago by Collin ▴ 1000
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1.5k
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Comment: C: How to go from VCF file to protein level
4.6 years ago by Collin ▴ 1000
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1.1k
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Comment: C: Mutation clustering in protein domains
4.6 years ago by Collin ▴ 1000
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1.5k
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Comment: C: How to download passenger mutations for cancer
4.7 years ago by Collin ▴ 1000
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1.5k
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Comment: C: How to download passenger mutations for cancer
4.7 years ago by Collin ▴ 1000
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1.5k
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Answer: A: How to download passenger mutations for cancer
4.7 years ago by Collin ▴ 1000
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6.1k
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Tool: CRAVAT: a web tool to annotate and analyze cancer variants
sequencing variant annotation Cancer
updated 2.8 years ago by 44k • written 9.1 years ago by ▴ 1000
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871
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Answer: A: Getting a list of tumor suppressors
4.7 years ago by Collin ▴ 1000
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4.1k
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Comment: C: Can't open file 'features': [Errno 2] No such file or directory
4.8 years ago by Collin ▴ 1000
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1
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4.1k
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Answer: A: Can't open file 'features': [Errno 2] No such file or directory
4.8 years ago by Collin ▴ 1000
2
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1
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1.3k
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Answer: A: Cancer driver mutations Identification from VCFs
4.8 years ago by Collin ▴ 1000
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1.3k
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
4.8 years ago by Collin ▴ 1000
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1.3k
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
4.8 years ago by Collin ▴ 1000
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3.2k
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Comment: C: Interesting things to do with 23andme data
4.8 years ago by Collin ▴ 1000
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692
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Answer: A: about snp prediction
4.8 years ago by Collin ▴ 1000
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1.3k
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Answer: A: Somatic Variant Annotation and Interpretation
4.8 years ago by Collin ▴ 1000
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4.8k
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Answer: A: Indel Annotation Tools, Not Loss Of Function
5.0 years ago by Collin ▴ 1000
1
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1
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5.1k
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Answer: A: How to "merge" monomeric structures in COOT (WinCoot) - pdb files
updated 5.0 years ago by 44k • written 9.0 years ago by ▴ 1000
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1
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2.7k
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Answer: A: Are there certain mutations ubiquitous in ALL cancers?
updated 5.0 years ago by 44k • written 9.0 years ago by ▴ 1000
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5.1k
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Comment: C: pathogenicity predictors of cancer mutations
5.4 years ago by Collin ▴ 1000
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4.5k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
5.4 years ago by Collin ▴ 1000
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4.5k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
5.4 years ago by Collin ▴ 1000
120 results • Page 1 of 3
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