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genomesport™is a whole genome test:
go further genotyping arrays


nowgenome™ low-pass whole genome sequencing technology delivers highly accurate variant calls across the whole genome


unlike common array-based genetic tests, with nowgenome™ we sequence and analyze your whole genome, using low pass technology, and our imputation and analysis software transforms sequencing reads into over 99% accurate variant calls across the whole genome

> 50x
more data than genotyping arrays
like 23andme

polygenic risk score calculations

Mobirise

> 99%
accurate variant calls across the whole genome

new variant discovery, CNV analysis, GWAS

1

library preparation

our library preparation method was developed specifically for low-pass sequencing, it is automated, resource efficient, and requires low amounts of input DNA

2

sequencing

we perform low-pass shotgun sequencing using the latest Illumina technology, and this results in an average of 50 times more measurements per genome than genotyping technologies

3

imputation & data analysis

we use imputation algorithms for sequencing data to call variants across the whole genome with high accuracy (average imputation r2 over 0.9), and, additionally, our standard data analysis includes ancestry and microbiome profiling of every sample


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genomesport
email: info@nilamedica.com 
© Copyright 2019 All rights reserved - Last update: 05/06/2019 
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Terms and Conditions

The genetic information provided by nowgenome are for wellness, information and educational uses and in no case must be used
for clinical or diagnostic purpose without the help of a medical doctor.
The information contained in this website and in the related sites are aimed at improving, and not replacing, the doctor-patient relationship.
None of the information provided in this website is intended to help to diagnose diseases and / or to indicate possible therapies.