Sandra Romain

About me

PhD holder in bioinformatics. I completed my PhD in the GenScale team from the Inria Center of the University of Rennes (France), under the supervision of Claire Lemaitre (Inria/IRISA) and Fabrice Legeai (INRAE).

I am currently looking for a Post-Doctoral position.

My PhD project

The heart of my project was to develop and implement methods for the identification and genotyping of genomic structural variants (SVs) using a pangenome representation. As a member of the Divalps ANR project team, I also performed data analysis on newly-produced long-read sequencing data from four species of Coenonympha butterfly, and worked towards the identification of large genomic rearrangements.

My PhD work can be divided into three main axes:

My full PhD thesis is available (in english) online: https://theses.hal.science/tel-04825910v1.

My PhD defense presentation slides: SandraRomain_PhD_Defense.pdf

Publications

Oral communications

Posters

Softwares

SVJedi-graph

SVJedi-graph is the first variation-graph-based long-read structural variant (SV) genotyper. It is inspired from SVJedi (Lecompte et al., 2020), a long-read SV genotyper that overcomes reference bias during read mapping by representing both alleles of bi-allelic SVs as independant sequences. The use of a variation-graph representation of the SVs in SVJedi-graph improves both the genotyping rate and accuracy of close and overlapping SVs compared to state of the art tools.

INVPG-annot

INVPG-annot is a tool that annotates inversion variants among the bubbles extracted from a pangenome graph.

Teaching experience

Other