Long read targeted sequencing enables genomic analysis of translocation hotspots in ...
PARDY, Filip, Veronika NAVRKALOVÁ, Kamila RÉBLOVÁ and Boris TICHÝ. Long read targeted sequencing enables genomic analysis of translocation hotspots in lymphoproliferative diseases. In Mendel Genetics Conference 2022. 2022. |
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Original name | Long read targeted sequencing enables genomic analysis of translocation hotspots in lymphoproliferative diseases |
Authors | PARDY, Filip, Veronika NAVRKALOVÁ, Kamila RÉBLOVÁ and Boris TICHÝ. |
Edition | Mendel Genetics Conference 2022, 2022. |
Other information | |
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Type of outcome | Conference abstract |
Confidentiality degree | is not subject to a state or trade secret |
Organization unit | Central European Institute of Technology |
Changed by | Changed by: Bc. Kateřina Kolesová, učo 112275. Changed: 18/8/2022 13:49. |
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LM2018132, large research infrastructures | Name: Národní centrum lékařské genomiky (Acronym: NCLG) |
Investor: Ministry of Education, Youth and Sports of the CR, National Center for Medical Genomics | |
NU22-08-00227, research and development project | Name: Pokročilé molekulární analýzy pro komplexní diagnostiku a monitorování pacientů s difúzním velkobuněčným B-lymfomem: využití profilování genové exprese, tekutých biopsií a sekvenování třetí generace |
Investor: Ministry of Health of the CR, Advanced molecular testing for aggregate diagnosis and management of DLBCL patients: engagement of gene expression profiling, liquid biopsy and long-read sequencing, Subprogram 1 - standard |
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