Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Genome graphs allow very general representations of genetic variation; depending on the model and implementation, variation at different length-scales (single nucleotide polymorphisms (SNPs), structural variants) and on different sequence backgrounds can be incorporated with different levels of transparency. We implement a model which handles this multiscale variation and develop a JSON extension of VCF (jVCF) allowing for variant calls on multiple references, both implemented in our software gramtools. We find gramtools outperforms existing methods for genotyping SNPs overlapping large deletions in M. tuberculosis and is able to genotype on multiple alternate backgrounds in P. falciparum, revealing previously hidden recombination.

Original publication

DOI

10.1186/s13059-021-02474-0

Type

Journal

Genome biology

Publication Date

09/2021

Volume

22

Addresses

EMBL-EBI, Hinxton, UK. bletcher@ebi.ac.uk.

Keywords

Humans, Plasmodium falciparum, Mycobacterium tuberculosis, Antigens, Surface, Reproducibility of Results, Sequence Deletion, Haplotypes, Polymorphism, Single Nucleotide, Alleles, Genome, Human, Algorithms, Computer Simulation, Genetic Variation, Genotyping Techniques