User: MMa

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MMa230
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Posts by MMa

<prev • 35 results • page 1 of 4 • next >
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How likely do cDNAs with start-loss variants appear in mRNA-seq?
... I know that many transcripts having frameshift mutations will be degraded by nonsense- or readthrough-mediated degradation, subject to rules that are well-known. How how about start-loss? Most likely they won't be translated if they don't have an alternate start codon, but will they be degraded qui ...
rna-seq written 4 months ago by MMa230
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Comment: C: Strategies to call variants from a cancer sample
... Well, the somatic callers I used (MuTect, MuTect2, VarScan, MuSE) do not call somatic reversions, which I hope they could. That aside, using only default parameters and nothing else on a particular pair I'm currently working, MuTect gives less than 2,000 variants and MuSE gives less than 500. I'd b ...
written 4 months ago by MMa230
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Comment: C: Strategies to call variants from a cancer sample
... I understand this. The purpose of the variant calling in question, however, is not to study their biological significance. I plan to do some RNA-editing research, so I need to identify DNA-level variations to act blacklist positions. ...
written 4 months ago by MMa230
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Comment: C: Strategies to call variants from a cancer sample
... Hi @igor, the intention is to identify all variants regardless of source. ...
written 4 months ago by MMa230
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Strategies to call variants from a cancer sample
... Hi all, I am looking to identify DNA-level variations from a matched tumor-normal WES data. Specifically, I just want to know the variations in the tumor sample in relate to the *reference genome*, not the normal sample. I have noticed two possible approaches here: 1. Simply use a germline-varia ...
next-gen snp written 4 months ago by MMa230 • updated 4 months ago by d-cameron1.5k
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Comment: C: Mapping between genomic coordinates to transcriptomic coordinates
... Eventually I got to try out this one. The important `GenomicFeatures` function here is `mapToTranscripts`: library(GenomicFeatures) library(rtracklayer) gencodeTxDb <- makeTxDbFromGFF (file="gencode.annotation.gtf") gencodeTx <- transcripts (gencodeTxDb) names (gencodeTx) ...
written 4 months ago by MMa230
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Answer: A: ssGSEA on RNA-Seq data from TCGA
... I know this is an old thread, but SSGSEA can be calculated using the Bioconductor package GSVA. If you use RPKM, use `ssgsea <- gsva (RPKM, method="ssgsea", kcdf="Gaussian", ...)`; if you use raw counts, use `ssgsea <- gsva (counts, method="ssgsea", kcdf="Poisson", ...)` ...
written 5 months ago by MMa230
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Comment: C: How to get sequencing depths from VCF with Rsamtools
... The docs for the current versions of pindel states depth is the same I'd get from `samtools depth`. ...
written 9 months ago by MMa230
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How to get sequencing depths from VCF with Rsamtools
... I got from our collaborator some pindel output and the BAM files that is used as pindel input. Unfortunately, they used an older of version of pindel (before approximately 0.2.4u) that doesn't record total depth at breakpoint (i.e. the DP field in VCF). While our collaborator's standard practice is ...
R rsamtools pindel written 9 months ago by MMa230 • updated 9 months ago by Pierre Lindenbaum106k
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Comment: C: bcftools: how to annotate a file with a larger file using bcftools annotate?
... If you did that successfully on a different file yesterday, then check whether the smallfile.vcf you're using today have been indexed. ...
written 9 months ago by MMa230

Latest awards to MMa

Teacher 8 months ago, created an answer with at least 3 up-votes. For A: Different results with edgeR when adding gene symbols
Teacher 11 months ago, created an answer with at least 3 up-votes. For A: Different results with edgeR when adding gene symbols
Scholar 11 months ago, created an answer that has been accepted. For C: I get the same modules but different number of genes WGCNA
Scholar 11 months ago, created an answer that has been accepted. For C: I get the same modules but different number of genes WGCNA

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