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759
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tool for calculate tumor-only sample purity of wgs or wes
next-gen genome
3.4 years ago by linouhao ▴ 10
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0
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967
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Comment: C: negative geo value analysis
3.6 years ago by linouhao ▴ 10
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13k
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Comment: C: series_matrix.txt in GEO are they always the normalized values?
3.6 years ago by linouhao ▴ 10
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1
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2.5k
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Comment: C: Noisy germline CNV data using CNVKit
updated 3.6 years ago by 11k • written 3.7 years ago by ▴ 10
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2
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967
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negative geo value analysis
microarray
updated 3.6 years ago by 11k • written 3.6 years ago by ▴ 10
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1
reply
13k
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Comment: A: series_matrix.txt in GEO are they always the normalized values?
updated 3.6 years ago by 11k • written 3.6 years ago by ▴ 10
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1
reply
4.7k
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Comment: C: Single-color and two color Agilent array analyzing in R
3.6 years ago by linouhao ▴ 10
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3.4k
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Comment: C: Why some microarray data have negative value? How to fix it?
3.6 years ago by linouhao ▴ 10
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3.6k
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Comment: C: CNVkit - how many normal samples do I need for the pooled normal reference?
3.7 years ago by linouhao ▴ 10
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0
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862
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Comment: C: CNV callers for WES data
3.7 years ago by linouhao ▴ 10
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1.2k
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Comment: C: Noisy CNV background in old FFPE sample
3.7 years ago by linouhao ▴ 10
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1.2k
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Comment: A: cnvkit filtering low depth bins
3.7 years ago by linouhao ▴ 10
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2.5k
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Comment: C: How are the log2 values in CNVkit .cnr files calculated?
3.7 years ago by linouhao ▴ 10
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0
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954
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how should I filter call.cns results according to cn depth p_ttest probes weight
cnv
3.7 years ago by linouhao ▴ 10
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982
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cnvkit suitable read depth , R version, reliable cutoff
cnvkit cnv
3.8 years ago by linouhao ▴ 10
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1
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11k
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Answer: A: Help with understanding CNVkit output
4.5 years ago by linouhao ▴ 10
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1
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1.2k
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Answer: A: Can CVNkit call CNV correctly at HLA genes region?
5.0 years ago by linouhao ▴ 10
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2
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4.7k
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Comment: A: bam_sort_core problem when bam files be processed by samtools
5.4 years ago by linouhao ▴ 10
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5.6k
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Comment: C: Why is normal blood used for matched tumor (instead of adjacent norm tissue)?
5.4 years ago by linouhao ▴ 10
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2.4k
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Comment: C: somatic variant calling with no germline sample
5.4 years ago by linouhao ▴ 10
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0
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2.4k
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Comment: C: somatic variant calling with no germline sample
5.4 years ago by linouhao ▴ 10
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1.7k
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Comment: C: CNV calling on tumor sample with no germline counterpart
5.4 years ago by linouhao ▴ 10
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2.5k
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Comment: C: Best CNV caller for Illumina WGRS data, in order to compare two phenotypes
5.4 years ago by linouhao ▴ 10
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0
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13k
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Comment: C: Finding Variable Genes in Seurat, scRNA-seq
5.5 years ago by linouhao ▴ 10
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0
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13k
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Comment: C: Finding Variable Genes in Seurat, scRNA-seq
5.5 years ago by linouhao ▴ 10
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0
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12k
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Comment: C: Can EdgeR of DeSeq be used for Single-cell RNA-seq?
5.5 years ago by linouhao ▴ 10
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3.0k
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Answer: A: How to adjust the position of chromosome or gene labels in OmicCircos
5.8 years ago by linouhao ▴ 10
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1
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50k
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Comment: C: Gene Set Clustering based on Functional annotation (GeneSCF)
5.8 years ago by linouhao ▴ 10
28 results • Page 1 of 1
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