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Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities
The rapid evolution and widespread use of next generation sequencing (NGS) in clinical laboratories has allowed an incredible progress in the genetic diagnostics of several inherited disorders. However, the new technologies have brought new challenges. In this review we consider the important issue...
保存先:
| 出版年: | EJIFCC |
|---|---|
| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The Communications and Publications Division (CPD) of the IFCC
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5949614/ https://ncbi.nlm.nih.gov/pubmed/29765282 |
| タグ: |
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