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Answer: Answer: Protein prediction tool
20 months ago by Collin ▴ 1000
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1.2k
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
21 months ago by Collin ▴ 1000
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1.2k
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Comment: Comment: Can non-driver mutations disrupt the function of proteins and further affect a c
21 months ago by Collin ▴ 1000
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2
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1.2k
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Answer: Answer: Can non-driver mutations disrupt the function of proteins and further affect a c
21 months ago by Collin ▴ 1000
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1.6k
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Answer: Answer: Identification of transcription factors from a list of DEGs
21 months ago by Collin ▴ 1000
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479
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Answer: Answer: Association analysis with SNP
22 months ago by Collin ▴ 1000
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980
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Comment: Comment: Preparing CHASMplus database for annotation
22 months ago by Collin ▴ 1000
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1
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980
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Comment: Comment: Preparing CHASMplus database for annotation
23 months ago by Collin ▴ 1000
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980
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Answer: Answer: Preparing CHASMplus database for annotation
23 months ago by Collin ▴ 1000
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2.9k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
24 months ago by Collin ▴ 1000
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2.9k
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Comment: Comment: Good annotation databases for a VCF file (somatic variants)
2.0 years ago by Collin ▴ 1000
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1.9k
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Answer: A: Is there a tool to predict if a missense variant causes a loss of function on th
updated 2.3 years ago by 129k • written 2.4 years ago by ▴ 1000
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2.3k
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Comment: C: VEP is very slow. Fork doesnt seem to work
2.3 years ago by Collin ▴ 1000
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2.3k
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Comment: C: VEP is very slow. Fork doesnt seem to work
2.3 years ago by Collin ▴ 1000
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1.9k
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Comment: C: Is there a tool to predict if a missense variant causes a loss of function on th
2.4 years ago by Collin ▴ 1000
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0
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23k
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Answer: Answer: SNP annotation tool
updated 16 months ago by 39k • written 2.6 years ago by ▴ 1000
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1.5k
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Comment: C: TCGA driver mutation data
2.6 years ago by Collin ▴ 1000
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1.2k
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Comment: C: Protein_Change in MAF
2.6 years ago by Collin ▴ 1000
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1.5k
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Comment: C: TCGA driver mutation data
2.6 years ago by Collin ▴ 1000
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1.5k
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Comment: C: TCGA driver mutation data
2.6 years ago by Collin ▴ 1000
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1.5k
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Comment: C: TCGA driver mutation data
2.6 years ago by Collin ▴ 1000
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1.5k
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Comment: C: TCGA driver mutation data
2.6 years ago by Collin ▴ 1000
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2
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1.5k
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Answer: C: TCGA driver mutation data
2.6 years ago by Collin ▴ 1000
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935
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
2.7 years ago by Collin ▴ 1000
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935
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Comment: C: Variant Calling scRNA-seq data for KRAS mutations
2.7 years ago by Collin ▴ 1000
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2.8k
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Comment: C: Get clinVar info for SNP with VEP
3.0 years ago by Collin ▴ 1000
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2.8k
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Comment: C: Get clinVar info for SNP with VEP
3.1 years ago by Collin ▴ 1000
2
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2
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2.8k
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Answer: C: Get clinVar info for SNP with VEP
3.1 years ago by Collin ▴ 1000
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849
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Comment: C: Variant effect prediction
3.1 years ago by Collin ▴ 1000
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1.1k
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Comment: C: How to go from VCF file to protein level
3.1 years ago by Collin ▴ 1000
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771
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Comment: C: Mutation clustering in protein domains
3.2 years ago by Collin ▴ 1000
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888
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Comment: C: How to download passenger mutations for cancer
3.2 years ago by Collin ▴ 1000
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888
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Comment: C: How to download passenger mutations for cancer
3.2 years ago by Collin ▴ 1000
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1
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888
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Answer: A: How to download passenger mutations for cancer
3.3 years ago by Collin ▴ 1000
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3
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5.5k
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Tool: CRAVAT: a web tool to annotate and analyze cancer variants
sequencing variant annotation Cancer
updated 15 months ago by 39k • written 7.6 years ago by ▴ 1000
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639
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Answer: A: Getting a list of tumor suppressors
3.3 years ago by Collin ▴ 1000
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1
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3.6k
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Comment: C: Can't open file 'features': [Errno 2] No such file or directory
3.3 years ago by Collin ▴ 1000
2
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1
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3.6k
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Answer: A: Can't open file 'features': [Errno 2] No such file or directory
3.3 years ago by Collin ▴ 1000
2
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1
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945
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Answer: A: Cancer driver mutations Identification from VCFs
3.3 years ago by Collin ▴ 1000
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0
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979
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
3.3 years ago by Collin ▴ 1000
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1
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979
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Comment: C: Suggested tool or algorithm for accessing pathogenicity and prioritization of so
3.3 years ago by Collin ▴ 1000
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2.5k
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Comment: C: Interesting things to do with 23andme data
3.3 years ago by Collin ▴ 1000
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480
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Answer: A: about snp prediction
3.3 years ago by Collin ▴ 1000
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1
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985
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Answer: A: Somatic Variant Annotation and Interpretation
3.4 years ago by Collin ▴ 1000
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4.1k
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Answer: A: Indel Annotation Tools, Not Loss Of Function
3.5 years ago by Collin ▴ 1000
1
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1
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4.5k
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Answer: A: How to "merge" monomeric structures in COOT (WinCoot) - pdb files
updated 3.5 years ago by 39k • written 7.5 years ago by ▴ 1000
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1
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2.2k
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Answer: A: Are there certain mutations ubiquitous in ALL cancers?
updated 3.5 years ago by 39k • written 7.5 years ago by ▴ 1000
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3.6k
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Comment: C: pathogenicity predictors of cancer mutations
3.9 years ago by Collin ▴ 1000
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3.1k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
3.9 years ago by Collin ▴ 1000
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3.1k
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Comment: C: Which Driver-Gene Detecting Software Supports hg38?
3.9 years ago by Collin ▴ 1000
120 results • Page 1 of 3
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