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Comment: C: No coverage or very low coverage in the Complete Genomics data
6.4 years ago by rse ▴ 100
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3.3k
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Comment: C: IGV Visualization Insert Size
6.4 years ago by rse ▴ 100
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1.4k
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Comment: A: Visualization software for large variations
6.4 years ago by rse ▴ 100
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6.1k
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Comment: C: Loss Of Heterozygosity Calls On Snp Annotated File
7.1 years ago by rse ▴ 100
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2.7k
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Comment: C: CNV / SV Filtration
7.1 years ago by rse ▴ 100
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2.7k
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Comment: C: CNV / SV Filtration
7.1 years ago by rse ▴ 100
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2.7k
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Comment: C: CNV / SV Filtration
7.1 years ago by rse ▴ 100
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2.4k
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Comment: Comment: SNVer error: chrome not found in Reference
7.8 years ago by rse ▴ 100
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4.3k
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Comment: C: Learn to develop bioinformatics tools
7.8 years ago by rse ▴ 100
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3.8k
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Comment: C: Retrieving gene names from list of mRNA accession IDs
7.9 years ago by rse ▴ 100
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9.9k
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Comment: C: gistic for whole genome sequencing copy number analysis
7.9 years ago by rse ▴ 100
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4.8k
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Comment: A: Why does GISTIC require a markers file?
7.9 years ago by rse ▴ 100
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3.4k
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Comment: C: Cnv Analysis After Segmentations
8.0 years ago by rse ▴ 100
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7.9k
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Comment: C: GISTIC 2.0 Segment CN
8.0 years ago by rse ▴ 100
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1
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9.9k
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Comment: C: gistic for whole genome sequencing copy number analysis
8.0 years ago by rse ▴ 100
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15k
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Comment: C: Extracting Individual Allele Frequencies From A Vcf File
8.0 years ago by rse ▴ 100
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4.0k
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Comment: C: Control-FREEC error message
8.0 years ago by rse ▴ 100
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1
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4.0k
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Comment: C: Control-FREEC error message
8.0 years ago by rse ▴ 100
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24k
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Comment: C: Tutorial: Analyze exome Copy number variation (CNV) in single patient or in popu
8.0 years ago by rse ▴ 100
1
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1
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7.9k
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Comment: A: GISTIC 2.0 Segment CN
8.0 years ago by rse ▴ 100
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1
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12k
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Comment: C: problems in hg19 and b37 compatibility
8.0 years ago by rse ▴ 100
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5.2k
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Comment: Comment: CNV tools for WGS data
updated 2.8 years ago by 43k • written 8.0 years ago by ▴ 100
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24k
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Comment: C: Tutorial: Analyze exome Copy number variation (CNV) in single patient or in popu
8.1 years ago by rse ▴ 100
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2
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24k
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Comment: C: Tutorial: Analyze exome Copy number variation (CNV) in single patient or in popu
8.1 years ago by rse ▴ 100
0
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1
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24k
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Comment: C: Tutorial: Analyze exome Copy number variation (CNV) in single patient or in popu
8.1 years ago by rse ▴ 100
0
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1
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24k
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Comment: A: Tutorial: Analyze exome Copy number variation (CNV) in single patient or in popu
8.1 years ago by rse ▴ 100
0
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1
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27k
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Comment: Comment: Converting Vcf File To Maf
updated 3.1 years ago by 43k • written 8.1 years ago by ▴ 100
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1
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6.8k
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Comment: Comment: Merging Bam Files
updated 22 months ago by 43k • written 9.1 years ago by ▴ 100
78 results • Page 2 of 2
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