Hi all
I recently made ATAC-seq libraries on two new cancer cell lines and I don't see nucleosomal pattern as I used to see in my previous library....
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Preferred analyzer for library size/library quality
Hello! I am new to the world of NGS and am curious about the preferred instrument for checking library quality. The ones that seem most popular are Agilent...
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MiSeq tolerated library size distribution
Our lab is trying some new library generation protocols where we are size selecting a much broader range of libraries than we have run previously, a 200...
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library depths for sequencing
Hi everybody,
I was approached by a biologist in our lab and was ask a specific question. As I was not really sure, I would like to share...
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Low concentration in TruSight One library preparation
Hi!
I encountered two problems while preparing Illumina's Trusight One library using their guide. I'm following the protocol carefully...
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library size calculation using DESeq1/2
Hello,
I would like to know if the lines at the end of the HTSeq file (which includes _no_feature, _ambiguous, _too_low_aQual, _not_aligned, and...
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Normalization of small RNA data for library size
Hi,
I have a few libraries of small RNA reads with different read counts: some libraries have more than 10 million reads, some others have <1...
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DESeq: estimateSizeFactors, library size estimation
I am working with high-throuput sequencing data and use DEseq to search for diff. exp. genes.
The protocol is somewhat similar to RNA-Seq, but...
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edgeR separate offset values/normalizations for each tag
Hi,
Thanks in advance for helping. I'm trying to use edgeR on some RNA-Seq data I have to test for differential expression. However, I...