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Tools

CCS calling

Convert raw PacBio sequencing reads into Circular Consensus Sequences

Haplotype calling

Perform haplotype calling from PacBio sequencing raw subreads against your own reference sequence

Service requests

Job tracker

Track the status of your current sequencing projects

Your jobs

Manage your current and past sequencing projects

Structural variant calling

Perform structural variant calling from genome-wide PacBio raw sequencing reads

Databases

Create new

Create a new database to perform population-wide variant calling using Sequegenics proprietary algorithms

Manage

Manage your databases

Launch new analysis

Launch haplotype-resolved variant calling of any region in the human genome

Query data

Explore and retrieve your mapped raw data and variant calling results. Connect to downstream analytics

S E Q U E G E N I C S