Bioconductor Readvcfasvranges

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somaticsignatures vranges readvcfasvranges

7.1 years ago guillaume.dachy • 0

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2.1k

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somaticsignatures somaticsignatures package readvcfasvranges vranges

8.2 years ago • updated 8.1 years ago guillaume.dachy • 0

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2.6k

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variantannotation readvcf readvcfasvranges vcf

updated 8.7 years ago by Michael Lawrence ★ 11k • written 8.7 years ago by ruben.drews • 0

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1.7k

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variantannotation readvcfasvranges vcf

updated 9.2 years ago by Michael Lawrence ★ 11k • written 9.2 years ago by Andy Lynch ▴ 120

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1.5k

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readvcfasvranges vcf to vranges

updated 9.3 years ago by Valerie Obenchain ★ 6.8k • written 9.3 years ago by arsala521 ▴ 10

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granges vranges readvcfasvranges somaticsignatures

updated 9.5 years ago by Michael Lawrence ★ 11k • written 9.5 years ago by jpluta26 • 0

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vcf readvcf readvcfasvranges

9.8 years ago Marcin Grzybowski • 0

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variantannotation filterVcf readvcfasvranges filterRules

updated 10.6 years ago by Martin Morgan 25k • written 10.6 years ago by Sigve Nakken ▴ 50

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variantannotation vranges readvcf readvcfasvranges metadata

10.6 years ago summerela • 0

9 results • Page 1 of 1

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Answer: DiffBind - question on the use of filtered or unfiltered input data by vejogos850 • 0

DiffBind - question on the use of filtered or unfiltered input data is the best to deal with, and it provides us the solutions that we are …

Answer: Help with defining groups by Gordon Smyth 53k

Defining sample groups is separate to reading in the DIA-NN data, because the sample conditions and covariates are not necessarily coded in…

Comment: Sharing a collection of datasets in ExperimentHub by Peter Hickey ▴ 760

The [**scRNAseq**](https://bioconductor.org/packages/scRNAseq/) package ([source on GitHub](https://github.com/LTLA/scRNAseq)) might serve …

Comment: Using DESeq2 on single cell RNA Seq data of same cell type but different conditi by ReinholdGaylord99 • 0

Thank you so much! https://www.nature.com/articles/s41467-021-25960-2/ [geometry dash lite](https://geometrydashlite.online)

Comment: Guidance on limma for pseudobulk scRNA-seq with multi-factor design by Gordon Smyth 53k

I'm not sure that I understand. You have a dataset that, even after pseudo-bulking, still has 6000 samples? That is surprising. Retaining …