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Comment: Create customized gene annotation file
Answer: MACS2 peak calling
Answer: How to determine the exact version of hg38 if I have only the FASTA file
PacBio Pipeline and Tools for Variant Call
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Comment: BioInformatics, Software
Answer: how to sort a fasta file
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Recent Replies
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Honestly, I am a fan of visualizing to select a threshold since these can depend on the specific experiment. I would even just run standard…
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Read all instructions carefully Specifically, this info is under the "Input JSON file specification" section with details in the followin…
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There have been some good suggestions, but it seems like you may be asking one of two questions, either (1) how to do bioinformatics? or (2…
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I'll follow up what a few others have mentioned, but I like stats.sh within the BBTools package for raw assembly stats. I'll then polish my…
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I agree this is very basic CRISPR mechanism and you'd be better off reading sites that could explain better than me. However, there is a lo…
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You want to use the MACS2 score columns? You can retain these with bedtools option `-c` . This will retain the score columns from any merge…
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The number of regions annotated as "Promoters" is the same regardless of TSS length? You can add this argument to annotatePeak (for mouse M…
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It is possible that NCBI keeps the entire `nr` indexes in memory and searches against that so there is no I/O involved. NCBI now also uses …
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10x does give you a big flashing warning telling you what the new default is, and tells you how to redo it without that if it's not what yo…
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smanzano250800
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Thank you, but it doesn´t work. I´ll try GeneSCF again.
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Organism: gallus gallus Genome version used: GRCg6a Chr and Position: NC_006113.5, 24618 Ref allele: A Alt allele: G Genotype: 1/1 (G/G) …
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Yeah, that's their assumption and also they assume that we're NOT *ONLY* interested in quantifying mature transcripts. However, for most an…
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apart from tool, is there any biological mechanism for explanation of interactions between different chromosomes?
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Yes, you would process sequencing and resequencing separately and then do a PCA. I would expect no relevant batch effect here.
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if you use `GenomicRanges::subtract(gr1, gr2) %>% unlist()` .. you'll get the `diff` without reduction
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