The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom
<br><strong>Purpose: </strong>The translation of genome sequencing into routine health care has been slow, partly because of concerns about affordability. The aspirational cost of sequencing a genome is $1000, but there is little evidence to support this estimate. We estimate the c...
Huvudupphovsmän: | Schwarze, K, Buchanan, J, Fermont, JM, Dreau, H, Tilley, MW, Taylor, JM, Antoniou, P, Knight, SJL, Camps, C, Pentony, MM, Kvikstad, EM, Harris, S, Popitsch, N, Pagnamenta, AT, Schuh, A, Taylor, JC, Wordsworth, S |
---|---|
Materialtyp: | Journal article |
Språk: | English |
Publicerad: |
Springer Nature
2019
|
Liknande verk
Liknande verk
-
Utility of whole-genome sequencing in the clinical diagnostic of rare inherited anaemias
av: C Camps, et al.
Publicerad: (2018) -
Diagnosing Burkitt lymphoma in sub-saharan Africa by sequencing of circulating tumour DNA: a comparative microcosting study
av: Morrell, L, et al.
Publicerad: (2025) -
Accurate costs of blood transfusion: a microcosting of administering blood products in the United Kingdom National Health Service
av: Stokes, E, et al.
Publicerad: (2018) -
Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencing
av: Schuh, A, et al.
Publicerad: (2018) -
Cost of hemophilia A in Brazil: a microcosting study
av: Ana Paula Beck da Silva Etges, et al.
Publicerad: (2024-08-01)