Example data for Cogent NGS software

Overview

Download raw sequencing data produced with next-generation sequencing (NGS) kits from Takara Bio to familiarize yourself with our user-friendly bioinformatics analysis tools, Cogent NGS Analysis Pipeline (CogentAP) and Discovery Software (CogentDS).

CogentAP and CogentDS are designed to analyze sequencing data generated using Takara Bio library preparation kits, including the Shasta Total RNA-Seq Kit, Shasta Whole-Genome Amplification (WGA) Kit, and plate-based mRNA-seq or total RNA-seq kits. These analysis tools are designed to be easy to use and accessible to any researcher, even with minimal prior bioinformatics experience.

Sign up below to access raw sequencing data generated with Takara Bio NGS kits. Login credentials to access the data will be provided via email. Datasets for the following library preparation kits are available for download:

Library preparation kit	Application	Sample information	Sequencing set-up	Data size
Shasta Total RNA-Seq	High-throughput single-cell total RNA profiling for up to 100,000 cells per run with full gene-body coverage	100,000 PBMCs (peripheral blood mononuclear cells)	Illumina® NovaSeq® PE150	7,819,525,231 PE (paired-end) reads in total 2 TB for raw FASTQ files for 100,000 cells 1.2 TB for demultiplexed 100,000 cells 126 GB for raw FASTQ files for 10,000 cells
Shasta WGA	High-throughput single-cell whole-genome amplification for up to 1,500 cells per run	1,500 immortalized cancer cells	Illumina NovaSeq PE151	427,688,062 PE reads in total 400 GB for FASTQ files
SMART-Seq Pro (Shasta mRNA-seq)	Single-cell full-length transcriptome analysis for up to 1,500 cells per run	714 PBMCs	Illumina NextSeq 1000	662,955,069 reads in total for SSPro_all_barcodes.bam 292.9 GB for SSPro_all_barcodes.bam NOTE: These files are available in .bam and .bai, not FASTQ, format.

Sign up below to access raw sequencing data

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