Cogent™ NGS Analysis Pipeline

Version 3.1

Overview

Cogent NGS Analysis Pipeline (also referred to as CogentAP) is bioinformatic software for analyzing single-cell RNA-seq, bulk RNA-seq, and single-cell DNA-seq data. Functionalities include gene or transcript expression counting, in silico ribodepletion, gene fusion detection, immune profiling analysis, and more. Please refer to the table in the bioinformatics resource portal for the full list of validated Takara Bio reagent kits supported for use with the pipeline. CogentAP inputs raw sequencing data and outputs an HTML report and other files, such as a gene matrix, to continue further analysis. Output also includes R data objects, which may be used as input for Cogent NGS Discovery Software.

Install the software to access the following features:

Command-line interface program
Mini-dataset files (WellList.txt and FASTQ files)—used to test the CogentAP functionality
Sample output reports and stats—used to compare to the analysis results of the mini-dataset test

Cat. #	Product	Size	Price	License	Quantity	Details
650005.V3.1	Cogent™ NGS Analysis Pipeline	Each	Inquire for Quotation		*
Notice to purchaser Our products are to be used for Research Use Only. They may not be used for any other purpose, including, but not limited to, use in humans, therapeutic or diagnostic use, or commercial use of any kind. Our products may not be transferred to third parties, resold, modified for resale, or used to manufacture commercial products or to provide a service to third parties without our prior written approval.

*You must be logged in to a Purchasing Account in order to purchase these products online, since the purchase of these products may be restricted depending on your account type. Researchers at not-for-profit accounts receive a limited use license with their purchase of the product. Researchers at for-profit accounts must obtain a license prior to purchase. For details please contact licensing@takarabio.com.

More Information

Supported operating systems

CogentAP can be installed on the following versions of Linux:

CentOS 8 or higher
Red Hat 8 or higher
Ubuntu 18.4 or higher

Hardware requirements

For analyzing Illumina NextSeq® High-Output data:

24-core CPU
64 GB+ RAM
1 TB available hard drive space*

Analyzing MiniSeq® or MiSeq® data may be possible on servers with less computational power than the specifications above. Analysis of HiSeq® or NovaSeq™ data would require better hardware than is listed.

*Data generated using the Shasta Total RNA-Seq Kit or Shasta Whole-Genome Amplification Kit requires at least six times the size of the input FASTQ files of free hard drive space for analyses with default parameters, and at least ten times the size of the input FASTQ files of free hard drive space for analyses including ribodepletion, immune profiling, and fusion analyses.

Additional third-party software dependencies*

Conda
bcl2fastq or BCL Convert for conversation of sequencer FASTQ output files

*Not included with the software; must be downloaded and installed separately.

Supported applications

See a list of supported applications.

Additional product information

More information is available in the Cogent NGS Analysis Pipeline User Manual or Quick Start Guide.

Cogent NGS Analysis Pipeline version history

Version number	Release date	Notes
CogentAP v3.1.27	2025-04-23	Minor bug fixes Corrections to the mitochondrial gene database for both human and mouse genomes Issue causing some ‘smartseq_fla_umi’ analysis runs to stop unexpectedly before the end of the run Issue where only R2 fastq reads were analyzed using FASTQC Issue with Shasta WGA analysis trim alignment default settings causing lower than expected alignment rates Issue on the WGA reporting that omitted some statistics from the HTML report if their value was zero (0) No changes to documentation
CogentAP v3.1.23	2025-04-02	Minor bug fixes Issue with demultiplexing which could lead to some barcodes/cells not being selected in rare cases when the number of reads for an experiment is very low and a given barcode represents a small fraction of the reads Issue with analysis where the incorrect reference file was used for the mouse genome for ribosomal depletion during the SortMeRNA process. This only affects analysis when the mouse genome is used as the reference. No changes to documentation
CogentAP v3.1	2025-01-15	Changes to install and upgrade procedure New pipeline framework (Nextflow) New DNA-seq analysis workflow, including CNV calling with Ginkgo New DNA-seq demux option Option to perform ribodepletion of data using SortMeRNA New kit data input options: Shasta Total RNA-Seq Kit and the Shasta Whole-Genome Amplification Kit
CogentAP 2.0.1	2023-05-26	Updated launch procedure Documentation: User Manual Quick Start Guide
CogentAP 2.0	2022-08-17	New plate-based kit data input option: SMART-Seq mRNA LP (with UMIs), SMART-Seq mRNA, and SMART-Seq mRNA LP (refer to the bioinformatics resources portal for a full list of supported kits) Documentation: User Manual Quick Start Guide
CogentAP 1.5.1	2022-03-25	New plate-based kit data input options Adds Nextera®- and TruSeq®-based adapter sequences for trimming New default gene fusion analysis filtering level to improve identification of true fusions New variable to customize filtering levels for gene fusion analysis (CLI-only) Minor bug fixes Documentation: User Manual Quick Start Guide
CogentAP 1.5	2021-12-03	Prerequisites: Requires Miniconda3 version 4.10.2 or higher Improved support for full-length transcriptomics, with additional options for transcript, gene fusion, and immune profiling analysis New kit data input options: SMART-Seq Pro Application Kit - 2 Chip Documentation: User Manual Quick Start Guide
CogentAP 1.0	2020-09-11	Prerequisites: Requires Miniconda3 version 4.8.2 or higher Requires bcl2fastq New kit data input options: ICELL8 Single-Cell System 3' DE for UMI workflow, SMARTer Stranded Total RNA-Seq Kit v3 - Pico Input Mammalian (includes UMIs) Documentation: User Manual Quick Start Guide
mappa Analyzer 1.0	2019-06-07	Prerequisites: Requires Miniconda3 version 4.5.0 or later Kit data input options: ICELL8 system sequencing results of full-length transcriptome or single-cell differential expression (3' DE or 5' DE) workflows, no UMI support Documentation: User Guide

More cells. More biomarkers. More discoveries.

Want to go from sample prep through data analysis with less hands-on time and stress? Meet the Shasta Single Cell System, which helps oncology researchers find novel biomarkers. Learn how our high-throughput Shasta technologies can inspire the next breakthrough.

Get the details

Sign up to get the Cogent NGS Analysis Pipeline

If you are interested in using CogentAP, please review the End User License Agreement (EULA) before populating the required fields of the form.

After checking the box to indicate acceptance of the EULA and submitting the completed form, your browser will be directed to a page where you can download the software. Installation instructions can be found in Cogent NGS Analysis Pipeline User Manual or Quick Start Guide.

Takara Bio USA, Inc.
United States/Canada: +1.800.662.2566 • Asia Pacific: +1.650.919.7300 • Europe: +33.(0)1.3904.6880 • Japan: +81.(0)77.565.6999
FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES. © 2025 Takara Bio Inc. All Rights Reserved. All trademarks are the property of Takara Bio Inc. or its affiliate(s) in the U.S. and/or other countries or their respective owners. Certain trademarks may not be registered in all jurisdictions. Additional product, intellectual property, and restricted use information is available at takarabio.com.