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Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiers.
Viailly PJ, Sater V, Viennot M, Bohers E, Vergne N, Berard C, Dauchel H, Lecroq T, Celebi A, Ruminy P, Marchand V, Lanic MD, Dubois S, Penther D, Tilly H, Mareschal S, Jardin F. Viailly PJ, et al. Among authors: lecroq t. BMC Bioinformatics. 2021 Mar 12;22(1):120. doi: 10.1186/s12859-021-04060-4. BMC Bioinformatics. 2021. PMID: 33711922 Free PMC article.
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. Mareschal S, et al. Among authors: lecroq t. Genes Chromosomes Cancer. 2016 Mar;55(3):251-67. doi: 10.1002/gcc.22328. Epub 2015 Nov 26. Genes Chromosomes Cancer. 2016. PMID: 26608593
Rgb: a scriptable genome browser for R.
Mareschal S, Dubois S, Lecroq T, Jardin F. Mareschal S, et al. Among authors: lecroq t. Bioinformatics. 2014 Aug 1;30(15):2204-5. doi: 10.1093/bioinformatics/btu185. Epub 2014 Apr 9. Bioinformatics. 2014. PMID: 24753490
Matching health information seekers' queries to medical terms.
Soualmia LF, Prieur-Gaston E, Moalla Z, Lecroq T, Darmoni SJ. Soualmia LF, et al. Among authors: lecroq t. BMC Bioinformatics. 2012;13 Suppl 14(Suppl 14):S11. doi: 10.1186/1471-2105-13-S14-S11. Epub 2012 Sep 7. BMC Bioinformatics. 2012. PMID: 23095521 Free PMC article.
27 results