Cargando…
Pitfalls of exome sequencing: a case study of the attribution of HABP2 rs7080536 in familial non-medullary thyroid cancer
Next-generation sequencing using exome capture is a common approach used for analysis of familial cancer syndromes. Despite the development of robust computational algorithms, the accrued experience of analyzing exome data sets and published guidelines, the analytical process remains an ad hoc serie...
Autores principales: | Gerhard, Glenn S., Bann, Darrin V., Broach, James, Goldenberg, David |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584869/ https://www.ncbi.nlm.nih.gov/pubmed/28884020 http://dx.doi.org/10.1038/s41525-017-0011-x |
Ejemplares similares
-
HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer
por: Weeks, Alexia L., et al.
Publicado: (2016) -
HABP2 G534E Variant in Papillary Thyroid Carcinoma
por: Tomsic, Jerneja, et al.
Publicado: (2016) -
HABP2 p.G534E variant in patients with family history of thyroid and breast cancer
por: Pinheiro, Maisa, et al.
Publicado: (2017) -
Pediatric Thyroid Cancer: To Whom Do You Send the Referral?
por: Keane, Allison, et al.
Publicado: (2021) -
Peptide receptor radionuclide therapy in patients with medullary thyroid carcinoma: predictors and pitfalls
por: Beukhof, Carolien M., et al.
Publicado: (2019)