Claire Lemaitre

Orcid: 0000-0001-8675-170X

According to our database1, Claire Lemaitre authored at least 20 papers between 2008 and 2025.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

Book  In proceedings  Article  PhD thesis  Dataset  Other 

Links

On csauthors.net:

Bibliography

2025
Mapler: a pipeline for assessing assembly quality in taxonomically rich metagenomes sequenced with HiFi reads.
Bioinform., 2025

Pairwise graph edit distance characterizes the impact of the construction method on pangenome graphs.
Bioinform., 2025

2023
MTG-Link: leveraging barcode information from linked-reads to assemble specific loci.
BMC Bioinform., December, 2023

SVJedi-graph: improving the genotyping of close and overlapping structural variants with long reads using a variation graph.
Bioinform., 2023

2021
Méthodes bioinformatiques pour l'étude des Variants de Structure avec des données de séquençages génomiques.
, 2021

2020
SVJedi: genotyping structural variations with long reads.
Bioinform., 2020

SimkaMin: fast and resource frugal de novo comparative metagenomics.
Bioinform., 2020

2017
De Novo NGS Data Compression.
Proceedings of the Algorithms for Next-Generation Sequencing Data, Techniques, 2017

2016
Multiple comparative metagenomics using multiset <i>k</i>-mer counting.
PeerJ Comput. Sci., 2016

2015
Reference-free compression of high throughput sequencing data with a probabilistic de Bruijn graph.
BMC Bioinform., 2015

2014
Compression of high throughput sequencing data with probabilistic de Bruijn graph.
CoRR, 2014

MindTheGap: integrated detection and assembly of short and long insertions.
Bioinform., 2014

GATB: Genome Assembly & Analysis Tool Box.
Bioinform., 2014

Mapping-Free and Assembly-Free Discovery of Inversion Breakpoints from Raw NGS Reads.
Proceedings of the Algorithms for Computational Biology - First International Conference, 2014

2012
Compareads: comparing huge metagenomic experiments.
BMC Bioinform., 2012

2011
A novel substitution matrix fitted to the compositional bias in Mollicutes improves the prediction of homologous relationships.
BMC Bioinform., 2011

2010
Cassis: detection of genomic rearrangement breakpoints.
Bioinform., 2010

2008
Réarrangements chromosomiques dans les génomes de mammifères : caractérisation des points de cassure. (Chromosomal rearrangements in mammalian genomes : characterising the breakpoints).
PhD thesis, 2008

A small trip in the untranquil world of genomes: A survey on the detection and analysis of genome rearrangement breakpoints.
Theor. Comput. Sci., 2008

Precise detection of rearrangement breakpoints in mammalian chromosomes.
BMC Bioinform., 2008


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