CountASAP: A Lightweight, Easy to Use Python Package for Processing ASAPseq Data.

Christopher T Boughter, Budhaditya Chatterjee,Yuko Ohta, Katrina Gorga, Carly Blair,Elizabeth M Hill, Zachary Fasana, Adedola Adebamowo, Farah Ammar, Ivan Kosik,Vel Murugan,Wilbur H Chen,Nevil J Singh,Martin Meier-Schellersheim

bioRxiv : the preprint server for biology(2024)

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Abstract
Declining sequencing costs coupled with the increasing availability of easy-to-use kits for the isolation of DNA and RNA transcripts from single cells have driven a rapid proliferation of studies centered around genomic and transcriptomic data. Simultaneously, a wealth of new techniques have been developed that utilize single cell technologies to interrogate a broad range of cell-biological processes. One recently developed technique, transposase-accessible chromatin with sequencing (ATAC) with select antigen profiling by sequencing (ASAPseq), provides a combination of chromatin accessibility assessments with measurements of cell-surface marker expression levels. While software exists for the characterization of these datasets, there currently exists no tool explicitly designed to reformat ASAP surface marker FASTQ data into a count matrix which can then be used for these downstream analyses. To address this, we created CountASAP, an easy-to-use Python package purposefully designed to transform FASTQ files from ASAP experiments into count matrices compatible with commonly-used downstream bioinformatic analysis packages. CountASAP takes advantage of the independence of the relevant data structures to perform fully parallelized matches of each sequenced read to user-supplied input ASAP oligos and unique cell-identifier sequences.
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