Whole Genome Resequencing – JEM BIORESEARCH

Whole Genome Re-Sequencing

Whole genome re-sequencing (WGR) compares the genomes of different individuals and populations to reference genomes to find variations in their genomes. These variations in the genome include single nucleotide polymorphisms (SNPs) and insertions-deletions (InDels). Whole genome re-sequencing can also detect larger genetic rearrangements, such as translocations, inversions, and copy number variations.

This method is used to find important traits and markers for inherited disorders, cancer mutations, disease outbreaks, and molecular breeding, as well as for improving agriculture and conservation efforts.

Enquiry Form

Kindly submit the form below for enquiries on whole genome re-sequencing, and our team will get back to you as soon as possible. *

Sequencing Service Type

Name

Contact Number

Company / Institut

Organism

Name of species in Latin

Genome size (no. of base pairs)

Sequencing Coverage (X)

Bioinformatics Required

Sequencing Platform

Message

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* Terms and conditions apply.