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3
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Answer: A: Free for academic use only licenses (If you want to sell your software please ju
5.0 years ago by Chris Miller 22k
1
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1
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2.4k
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Answer: A: HGVS format to VCF from portal.gdc.cancer.gov
5.0 years ago by Chris Miller 22k
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8.2k
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Answer: A: Saving 3D plot from rgl as a pdf
5.1 years ago by Chris Miller 22k
2
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1
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3.1k
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Answer: A: CNVkit: Choice of Bin Size and CNV Calling
5.2 years ago by Chris Miller 22k
3
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2.3k
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Answer: A: Reproducing this picture
5.2 years ago by Chris Miller 22k
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1.5k
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Answer: A: Detecting known, low frequency SNPs in bacterial populations
5.3 years ago by Chris Miller 22k
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1.3k
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Answer: A: Does sciClone work on mouse exome data?
5.3 years ago by Chris Miller 22k
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1.3k
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Answer: A: SciClone works with 1d clustering, but not 2d?
5.3 years ago by Chris Miller 22k
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1.2k
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Answer: A: regions with very different VAF fall into one cluster
5.3 years ago by Chris Miller 22k
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2.1k
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Answer: A: Convert indel list with [-/A] notation to VCF with adjacent base
5.3 years ago by Chris Miller 22k
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1.5k
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Answer: A: Cancer Genomics and Bioinformatics positions at WashU (Griffith Lab)
5.4 years ago by Chris Miller 22k
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1.6k
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Answer: A: Postdoc position in single-cell cancer genomics
5.4 years ago by Chris Miller 22k
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1.2k
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Answer: A: Get Flanking Amino Acid Sequence
5.4 years ago by Chris Miller 22k
2
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1.5k
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Answer: A: Getting same SNPs both in cancer and normal files when seen in IGV - Integrativ
5.4 years ago by Chris Miller 22k
1
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1
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2.2k
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Answer: A: a question about fishplot
5.5 years ago by Chris Miller 22k
1
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4.4k
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Answer: A: How to load BAM files that do not have chromosome name in the header?
5.5 years ago by Chris Miller 22k
1
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4.6k
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Answer: A: How can I find motifs under individual ATAC-peaks?
5.6 years ago by Chris Miller 22k
1
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1
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3.7k
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Answer: A: Where are mutation files (MAF) for TCGA normal samples on Firebrowse
5.6 years ago by Chris Miller 22k
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1.2k
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Answer: A: Calling CNVs from WGS data
5.6 years ago by Chris Miller 22k
2
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1
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2.9k
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Answer: A: Running sciClone on cell prevalence (CP) data
updated 5.6 years ago by 43k • written 8.2 years ago by 22k
2
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0
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2.2k
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Answer: A: Is there a database which gives meta-level information of mutation(both nuclueot
updated 5.6 years ago by 43k • written 8.2 years ago by 22k
1
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0
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6.7k
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Answer: A: R phangorn phylogenetic analysis from somatic mutations' binary table
updated 5.6 years ago by 43k • written 8.2 years ago by 22k
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0
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1.8k
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Answer: A: sciClone annotation file
updated 5.6 years ago by 43k • written 8.2 years ago by 22k
2
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1
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4.4k
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Answer: A: Extracting Reads by position
updated 5.6 years ago by 43k • written 8.2 years ago by 22k
0
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2
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17k
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Answer: A: Writing Collaboration With Source-Control And Microsoft-Word
updated 5.6 years ago by 43k • written 13.8 years ago by 22k
1
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0
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2.8k
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Answer: A: What Is The Statistical Framework To Compare Distribution Of Two Samples Of Geno
updated 5.6 years ago by 43k • written 13.8 years ago by 22k
1
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0
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12k
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Answer: A: Statistics: Combinations In Python
updated 5.6 years ago by 43k • written 13.9 years ago by 22k
4
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0
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7.4k
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Answer: A: How Can I Read The Contents Of Rdata!, Where Is It Located ? And How Can I Acces
updated 5.6 years ago by 43k • written 13.9 years ago by 22k
1
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0
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1.9k
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Answer: A: Plotting Lines Of A Table In R
updated 5.6 years ago by 43k • written 13.9 years ago by 22k
3
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1
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8.4k
views
Answer: A: Rearranging Dna Sequences
updated 5.6 years ago by 43k • written 14.1 years ago by 22k
5
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4
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23k
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Answer: Answer: How Do I Access And Query Entire Genome Sequences With R
updated 5 months ago by 43k • written 14.1 years ago by 22k
1
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0
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1000
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Answer: A: high frequency SNPs (and other variations) after subtracting blood variants from
5.8 years ago by Chris Miller 22k
3
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2.2k
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Answer: A: Should bioinformaticians learn the scientific names of plants and animals?
5.8 years ago by Chris Miller 22k
3
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1.2k
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Answer: A: How to distinguish methylated cytosine and unmethylathed cytosine?
5.8 years ago by Chris Miller 22k
3
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0
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2.3k
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Answer: A: Neoantigen prediction Tools
5.8 years ago by Chris Miller 22k
0
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0
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992
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Answer: A: Clonal evolution for samples with no common CNV
5.9 years ago by Chris Miller 22k
1
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1
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1.9k
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Answer: A: SciClone: Why cluster in non-CN neutral region considering it infers only on CN
5.9 years ago by Chris Miller 22k
1
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0
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2.0k
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Answer: A: Sciclone took too long
5.9 years ago by Chris Miller 22k
1
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0
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3.2k
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Answer: A: Sciclone clonevol integration
5.9 years ago by Chris Miller 22k
1
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0
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1.2k
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Answer: A: Can sciclone handle multiallelic variants?
5.9 years ago by Chris Miller 22k
0
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0
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1.4k
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Answer: A: somaticsniper VAF calclulation
5.9 years ago by Chris Miller 22k
1
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1
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1.3k
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Answer: A: How can you sort variants based on their positions from upstream to downstream?
6.1 years ago by Chris Miller 22k
1
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0
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2.4k
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Answer: A: IGV - is there a way to extract bulk information?
6.1 years ago by Chris Miller 22k
1
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0
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4.9k
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Answer: A: samtools view: failed to open "sort" for reading: No such file or directory
updated 6.1 years ago by 43k • written 6.1 years ago by 22k
1
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1
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2.3k
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Answer: A: WGS coverage (depth) for CNV detection
6.2 years ago by Chris Miller 22k
0
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1.2k
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Answer: A: Does sequence length matter for CNV and variants?
6.2 years ago by Chris Miller 22k
0
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2.6k
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Answer: A: SciClone: Tumor purity estimation
6.2 years ago by Chris Miller 22k
1
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1
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1.7k
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Answer: A: Mapping Protein Mutation to Genomic DNA
6.2 years ago by Chris Miller 22k
0
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0
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3.2k
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Answer: A: Indel concordance from different VCF files
6.2 years ago by Chris Miller 22k
2
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1
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4.2k
views
Answer: A: Saving IGV images for bigwig files
6.2 years ago by Chris Miller 22k
478 results • Page 2 of 10
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