D Oh, JS Strattan, JK Hur, J Bento, AE Urban, G Song… - Scientific reports, 2020 - nature.com
ChIP-seq is one of the core experimental resources available to understand genome-wide epigenetic interactions and identify the functional elements associated with diseases. The …
Abstract Motivation Unique molecular identifiers (UMIs) are added to DNA fragments before PCR amplification to discriminate between alleles arising from the same genomic locus and …
A key step in the transformation of raw sequencing reads into biological insights is the trimming of adapter sequences and low-quality bases. Read trimming has been shown to …
Next-generation sequencing: adjusting to data overload | Nature Methods Skip to main content Thank you for visiting nature.com. You are using a browser version with limited support for …
The year 2022 will be remembered as the turning point for accurate long-read sequencing, which now establishes the gold standard for speed and accuracy at competitive costs. We …
Assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq) is a technique widely used to investigate genome-wide chromatin accessibility. The recently …
M Mohiyuddin, JC Mu, J Li, N Bani Asadi… - …, 2015 - academic.oup.com
Structural variations (SVs) are large genomic rearrangements that vary significantly in size, making them challenging to detect with the relatively short reads from next-generation …
E Blanco, M González-Ramírez, L Di Croce - Scientific Reports, 2021 - nature.com
Large-scale sequencing techniques to chart genomes are entirely consolidated. Stable computational methods to perform primary tasks such as quality control, read mapping, peak …
Y Chen, S Chen, EP Lei - Bioinformatics, 2022 - academic.oup.com
Motivation ChIP-seq detects protein–DNA interactions within chromatin, such as that of chromatin structural components and transcription machinery. ChIP-seq profiles are often …