A PLATFORM TO HELP YOU IMPLEMENT PACBIO SEQUENCING FOR YOUR POPULATION GENOMICS PROJECT, WITH INTEGRATED BIONFORMATICS TOOLS FOR GENOME MAPPING, VARIANT CALLING, AND FILE FORMAT CONVERSION FOR DOWNSTREAM BIG DATA ANALYTICS
Upload your raw sequencing data
Create and manage biosamples in the cloud. Upload large .subreads.bam files directly from your machine. Organize your data by sample, sequencing run, and link metadata to add more granularity to your analysis. Get your data automatically mapped against a reference genome sequence and cataloged by position.
Launch a new analysis
Launch targeted variant calling analysis over any gene from the list of all 20,000+ genes in the human genome, or define your own genomic region to target. Launch every coding region, or the entire genome in one click. Use our proprietary approach to improve sensitivity for variant calling from low coverage data.
Upload more data to build databases
Keep your data organized across databases, and facilitate rapid population-level analysis.
Launch a population analysis
Using Sequegenics' proprietary tools for population genomics, rapidly perform population-level analysis to seek for correlates to any covariate submitted in the metadata.
Use this simple reference-guided approach to convert noisy long-read NGS raw data into high-quality DNA sequences
1- Upload your raw data
2- Upload your reference sequence
3- Upload the fastq file of raw subreads
4- Launch your analysis
Produce accurate variant calling from WGS data for any human gene in only a few clicks
Our WGS application is a centralized solution that let you access raw data from your own databases and rapidly process it to extract high quality DNA sequences from any region in the human genome.
A fully automated analytical solution
Minimize the time spent on variant calling and get haplotype-resolved variants minutes after uploading your raw data.
Go straight into downstream analytics and speed up discovery