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A: Using A Variable As A Blocking Factor Vs Putting It As A Term In The Model Formu
Answer: Before or after LD clumping for PRS calculation in GWAS
Comment: CAZy database has multiple family sequence...
RNA-seq differential expression across multiple tissues, 2 trials, and 2 conditions
Answer: Differential express genes in imbalance groups
Answer: Differential express genes in imbalance groups
Comment: Differential express genes in imbalance groups
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Recent Replies
Answer: Subsetting Seurat object based on list of cell barcodes
by
fracarb8
★ 1.5k
`subset(seurat.obj_combined, cells = all_good_cells_rhemac10$V1)` You need to pass `cells` not `subset`. From the documentation: sub…
Answer: TCGA UUIDS to TCGA barcode (SampleID) in R
by
aUser
▴ 30
Great solutions on this page, the old web page has been replace with new one, so you need to use the new link, and it will work: old lin…
Comment: Issues With Cram -> Fastq from GTEx v8 WGS
by
Pierre Lindenbaum
160k
unless your cram in sorted on query rather than on coordinate, your cram must be first sort processed with collate: https://twitter.com/lh…
Comment: error in wigToBigWig while converting mappability to bedgraph
by
Pierre Lindenbaum
160k
remove the spaces from your "chrom" key variableStep chrom=NT_173277 span=5 or may be quote the chrom variableStep chrom="NT_173277.1 C…
Comment: DEG (Differential expression gene) analysis
by
dsull
★ 5.6k
Well, I guess expression could be measured from the DNA indirectly such as with RNA Pol II binding to DNA via ChIP-seq but then the OP shou…
Answer: DEG (Differential expression gene) analysis
by
dsull
★ 5.6k
What exactly is "DNA-level DEG"? That makes zero sense. DEG = Differential **EXPRESSION** of genes. In any case, for RNA sequencing data, …
Answer: Biobambam vs Picard in RNA Sequencing Analysis for BAM to FASTQ
by
Zhenyu Zhang
★ 1.1k
Let me say even if you had used the exactly same bioinformatics steps, you will still have batch efforts from sample collection, storage an…
Comment: Before or after LD clumping for PRS calculation in GWAS
by
경준
▴ 20
1. I think i misunderstood logistic regression of association test. Now I understand. 2. you're right. Thank you for your helpful reply sam…
Comment: library(scater)
by
Mensur Dlakic
★ 26k
> I am not able to install the package scater as per the webpage I urge you to read back what you wrote and think whether you'd be able to…
Comment: How to corrected test statistics based on the LDSC intercept?
by
Isaac
• 0
Thank you very much!
Comment: Transcription Start Site
by
Ming Tommy Tang
★ 3.8k
you can use bioconductor as shown in this post using Genomicanges https://support.bioconductor.org/p/46508/
Comment: scRNAseq normalization
by
Ming Tommy Tang
★ 3.8k
To be honest, I really do not use SCT, and use log normalization all the time...
Comment: Subsetting Seurat object based on list of cell barcodes
by
Ming Tommy Tang
★ 3.8k
index<- rownames(seurat.obj_combined) %in% all_good_cells_rhemac10$V1 seurat.obj_combined[index, ] should do the trick
Comment: Average expression of a sample in single-cell data
by
dsull
★ 5.6k
Well, if you're only sequencing the very end (the 3' end) of transcripts, how are you going to detect any of the splice junctions that appe…
Answer: Is it better to pool samples prior to running deseq2, or should the algorithm be
by
swbarnes2
14k
> Seems like pooling all should be statistically more robust. Yup. So put everything into the same DESeq2 object. See: https://…
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