Format
Sort by

Send to

Choose Destination

Search results

Items: 15

1.

Whole exome sequencing of relapsed/refractory patients expands the repertoire of somatic mutations in diffuse large B-cell lymphoma.

Mareschal S, Dubois S, Viailly PJ, Bertrand P, Bohers E, Maingonnat C, Jaïs JP, Tesson B, Ruminy P, Peyrouze P, Copie-Bergman C, Fest T, Jo Molina T, Haioun C, Salles G, Tilly H, Lecroq T, Leroy K, Jardin F.

Genes Chromosomes Cancer. 2016 Mar;55(3):251-67. doi: 10.1002/gcc.22328. Epub 2015 Nov 26.

PMID:
26608593
2.

A fast Boyer-Moore type pattern matching algorithm for highly similar sequences.

Ben Nsira N, Lecroq T, Elloumi M.

Int J Data Min Bioinform. 2015;13(3):266-88.

PMID:
26547980
3.
4.

Managing large-scale genomic datasets and translation into clinical practice.

Lecroq T, Soualmia LF.

Yearb Med Inform. 2014 Aug 15;9:212-4. doi: 10.15265/IY-2014-0039.

5.

Rgb: a scriptable genome browser for R.

Mareschal S, Dubois S, Lecroq T, Jardin F.

Bioinformatics. 2014 Aug 1;30(15):2204-5. doi: 10.1093/bioinformatics/btu185. Epub 2014 Apr 9.

6.

From genome sequencing to bedside. Findings from the section on bioinformatics and translational informatics.

Lecroq T, Soualmia LF; Section Editors for the IMIA Yearbook Section on Bioinformatics and Translational Informatics.

Yearb Med Inform. 2013;8:175-7. Review.

PMID:
23974568
7.

Querying highly similar sequences.

Barton C, Giraud M, Iliopoulos CS, Lecroq T, Mouchard L, Pissis SP.

Int J Comput Biol Drug Des. 2013;6(1-2):119-30. doi: 10.1504/IJCBDD.2013.052206. Epub 2013 Feb 21.

PMID:
23428478
8.

EVA: Exome Variation Analyzer, an efficient and versatile tool for filtering strategies in medical genomics.

Coutant S, Cabot C, Lefebvre A, Léonard M, Prieur-Gaston E, Campion D, Lecroq T, Dauchel H.

BMC Bioinformatics. 2012;13 Suppl 14:S9. doi: 10.1186/1471-2105-13-S14-S9. Epub 2012 Sep 7.

9.

Matching health information seekers' queries to medical terms.

Soualmia LF, Prieur-Gaston E, Moalla Z, Lecroq T, Darmoni SJ.

BMC Bioinformatics. 2012;13 Suppl 14:S11. doi: 10.1186/1471-2105-13-S14-S11. Epub 2012 Sep 7.

10.

Extraction of infrequent simple motifs from a finite set of sequences using a lattice structure.

El-Falah T, Lecroq T, Elloumi M.

Recent Pat DNA Gene Seq. 2013 Aug;7(2):123-7.

PMID:
22974262
11.

Querying large read collections in main memory: a versatile data structure.

Philippe N, Salson M, Lecroq T, Léonard M, Commes T, Rivals E.

BMC Bioinformatics. 2011 Jun 17;12:242. doi: 10.1186/1471-2105-12-242.

12.

An automated approach to map a French terminology to UMLS.

Merabti T, Massari P, Joubert M, Sadou E, Lecroq T, Abdoune H, Rodrigues JM, Darmoni SJ.

Stud Health Technol Inform. 2010;160(Pt 2):1040-4.

PMID:
20841842
13.

Projection and inheritance of SNOMED CT relations between MeSH terms.

Merabti T, Letord C, Abdoune H, Lecroq T, Joubert M, Darmoni SJ.

Stud Health Technol Inform. 2009;150:233-7.

PMID:
19745303
14.

Searching related resources in a quality controlled health gateway: a feasibility study.

Merabti T, Pereira S, Letord C, Lecroq T, Joubert M, Dahamna B, Darmoni SJ.

Stud Health Technol Inform. 2008;136:235-40.

PMID:
18487737
15.

FORRepeats: detects repeats on entire chromosomes and between genomes.

Lefebvre A, Lecroq T, Dauchel H, Alexandre J.

Bioinformatics. 2003 Feb 12;19(3):319-26.

Items per page

Supplemental Content

Loading ...
Write to the Help Desk