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Answer: What is the best way to clean bulk RNA-seq data?
Answer: NCBI refseq ids to uniprot ids
Answer: NCBI refseq ids to uniprot ids
Comment: Unusual FASTQ file
Answer: Graphing Average Expression of Group of Genes
Comment: Graphing Average Expression of Group of Genes
How to create specific .bed files for a panel of genes
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Recent Replies
Comment: How to deal with duplicated gene IDs in TCGA RNA expression data?
by
Vincent Laufer
★ 2.8k
I also said that on this forum xD. But anyway, actually its probably not impossible. What I would do is first read through [the FAQ][1], …
Comment: How to deal with duplicated gene IDs in TCGA RNA expression data?
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Camilo Andres
▴ 30
few of them, like 25, according to Gene_Entrez_IDs. They are the data from the pancancer project corresponding to breast invasive carcinoma…
Comment: BCR/TCR analysis using target capture sequencing data
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J.F.Jiang
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Thanks, Jesse We designed the probes based on the genomic sequences of V/D/J genes within the TCR/BCR loci. I've tried both IgBlast and M…
Answer: I don't want to believe the Interproscan DB estimated download time.
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Mensur Dlakic
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With [**aria2**][1] and multiple connections, I download at ~2.2MiB. The estimate is still ~190 hours. aria2c --continue=true --max-…
Comment: Seurat: How to get all genes name of a cell ?
by
jv
★ 1.2k
if you want the genes in your count matrix use `rownames(obj)`. Or are you looking to get all genes with count > 0 for a particular cell? P…
Comment: Unusual FASTQ file
by
Ram
39k
People from the middle east/indian subcontinent often associate the term "post title" with their job title, because a) post translates more…
Comment: How to make a dotplot for bulk RNA average expression ?
by
bhumm
▴ 40
I am not entirely clear on what you are trying to accomplish, but based on @Trivas answer, I would first transform the data relative to ave…
Answer: What is the best way to clean bulk RNA-seq data?
by
swbarnes2
13k
There really is no "best". Just find something reasonable, and document what you chose.
Comment: How to deal with duplicated gene IDs in TCGA RNA expression data?
by
Vincent Laufer
★ 2.8k
ok interesting. Do all, most, some, or a few of the genes have repeated lines. Is there a handy link to the exact file you are looking at?
Answer: Make a BedGraph file
by
bhumm
▴ 40
Bedtools window piped into genomecov? https://bedtools.readthedocs.io/en/latest/content/tools/window.html https://bedtools.readthedocs.io…
Answer: RNAseq Data and Pipeline
by
ATpoint
72k
STAR counts are the raw counts, that is appropriate for DESeq2.
Comment: RNAseq Data and Pipeline
by
swbarnes2
13k
STAR has a GeneCounts output that looks as you describe; three columns, depending on whether one thinks the prep is unstranded, or stranded…
Comment: RNAseq Data and Pipeline
by
Ram
39k
There is at least one more step that you haven't shared, isn't there? This line alone does not get you the data. You don't need to give us …
Comment: RNAseq Data and Pipeline
by
turcoa1
• 0
my entire code is not done. All I am trying to understand is if the STAR - counts downloaded from this query have raw reads. There are head…
Comment: RNAseq Data and Pipeline
by
Ram
39k
Please provide your entire code so those of us wishing to do a quick test can download and check for ourselves. Also, please use the format…
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