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Answer: Answer: InferCNV results interpretation
7 months ago by arno.guille ▴ 410
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4.6k
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Answer: A: CBS segmentation with DNAcopy taking ages/hanging
updated 4.3 years ago by 43k • written 10.0 years ago by ▴ 410
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1
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1.6k
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Answer: Answer: How to convert segmented aCGH probe-based to gene-based?
updated 19 months ago by 43k • written 8.6 years ago by ▴ 410
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Answer: A: Software to analyse mutations in sanger sequencing files
8.3 years ago by arno.guille ▴ 410
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7.6k
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Answer: Answer: Is there a database linking cell lines and mutations?
updated 19 months ago by 43k • written 8.6 years ago by ▴ 410
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9.3k
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Comment: C: BWA alignment using paired end reads from different lanes
9.0 years ago by arno.guille ▴ 410
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9.3k
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Comment: Comment: BWA alignment using paired end reads from different lanes
updated 22 months ago by 43k • written 9.1 years ago by ▴ 410
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9.3k
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Comment: Comment: BWA alignment using paired end reads from different lanes
updated 22 months ago by 43k • written 9.1 years ago by ▴ 410
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9.3k
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Comment: C: BWA alignment using paired end reads from different lanes
9.1 years ago by arno.guille ▴ 410
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3.7k
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Answer: A: Unix or Linux which is better choice for genomic analysis?
9.2 years ago by arno.guille ▴ 410
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Answer: Answer: Can you automatically detect if reads are from Illumina or IonTorrent?
updated 2.2 years ago by 43k • written 9.5 years ago by ▴ 410
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1
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5.9k
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Answer: Answer: hg19_cosmic_v54_120711.vcf for mutect analysis
updated 2.2 years ago by 43k • written 9.5 years ago by ▴ 410
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10k
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Comment: Comment: Annotating variants with Annovar, Oncotator and SnpEFF
updated 3.0 years ago by 43k • written 9.5 years ago by ▴ 410
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10k
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Comment: Comment: Annotating variants with Annovar, Oncotator and SnpEFF
updated 3.0 years ago by 43k • written 9.5 years ago by ▴ 410
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Comment: Comment: question about drawing heatmap with R
updated 3.1 years ago by 43k • written 9.5 years ago by ▴ 410
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1
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5.5k
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Answer: Answer: question about drawing heatmap with R
updated 3.1 years ago by 43k • written 9.5 years ago by ▴ 410
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0
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3.2k
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Comment: Comment: Problem generating VCFs from MuTect variant caller
updated 2.3 years ago by 43k • written 9.6 years ago by ▴ 410
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4.3k
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Comment: C: Annotation using annovar
9.7 years ago by arno.guille ▴ 410
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4.3k
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Comment: Comment: Annotation using annovar
updated 2.3 years ago by 43k • written 9.7 years ago by ▴ 410
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4.3k
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Comment: A: Annotation using annovar
9.7 years ago by arno.guille ▴ 410
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4.3k
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Answer: A: Annotation using annovar
9.7 years ago by arno.guille ▴ 410
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4.3k
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Answer: A: Pearson’S Correlation Method In R
10.2 years ago by arno.guille ▴ 410
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8.1k
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Comment: C: How To Retrieve Reads Supporting A Snp/Indel
10.3 years ago by arno.guille ▴ 410
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Comment: C: Hypergeometric Test On Gene Set
10.3 years ago by arno.guille ▴ 410
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Comment: Comment: Hypergeometric Test On Gene Set
updated 13 months ago by 43k • written 10.3 years ago by ▴ 410
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Answer: A: How To Calculate Degree Of Deletion And Amplification Of Cnv Given Snp Array Dat
10.6 years ago by arno.guille ▴ 410
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1
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8.7k
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Comment: C: Very High Percentage Of Reads Are Pcr Duplicates - Iontorrent
10.6 years ago by arno.guille ▴ 410
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1
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8.7k
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Answer: C: Very High Percentage Of Reads Are Pcr Duplicates - Iontorrent
10.6 years ago by arno.guille ▴ 410
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2.9k
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Answer: A: How To Handle The Case A Affymetrix Probe Set Id Mapped To Multiple Genes?
10.7 years ago by arno.guille ▴ 410
6
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1
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30k
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Answer: A: Where To Download Pam50 Gene Set?
10.7 years ago by arno.guille ▴ 410
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1.9k
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Answer: A: Visualization Of Cnvs
11.6 years ago by arno.guille ▴ 410
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