1- To generate a sequencing library of transcriptome, the cellular is converted to a library followed by and ligation of . A defined range of the fragments are further purified for the following high throughput
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1- To generate a sequencing library of transcriptome, the cellular is converted to a library followed by and ligation of . A defined range of the fragments are further purified for the following high throughput .
2- To identify genes from sequencing data, read sequences are either ___________ to a reference genome or by de novo _____________.
3- is a normalization procedure of read counts data from sequencing, which the of read counts of a transcript is adjusted for the of the transcript and by in a sequence run.
4- To identify differentially expressed genes using whole transcriptome analysis, it is essential to test for ____________ significance with ____________ corrections of genomic data.
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