Novel bioinformatic developments for exome sequencing.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 603, doi. 10.1007/s00439-016-1658-6
- By:
- Publication type:
- Article
Works matching IS 03406717 AND DT 2016 AND VI 135 AND IP 6
Results: 8
1
2
Discovery of mutations for Mendelian disorders.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 615, doi. 10.1007/s00439-016-1664-8
- By:
- Publication type:
- Article
3
A Clinician's perspective on clinical exome sequencing.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 643, doi. 10.1007/s00439-016-1662-x
- By:
- Publication type:
- Article
4
Deciphering intratumor heterogeneity using cancer genome analysis.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 635, doi. 10.1007/s00439-016-1670-x
- By:
- Publication type:
- Article
5
Regulating whole exome sequencing as a diagnostic test.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 655, doi. 10.1007/s00439-016-1677-3
- By:
- Publication type:
- Article
6
Discovery of rare variants for complex phenotypes.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 625, doi. 10.1007/s00439-016-1679-1
- By:
- Publication type:
- Article
7
The journey of exome sequencing from disease mutations discovery to clinical genomics.
- Published in:
- 2016
- By:
- Publication type:
- Editorial
8
Clinical genomics: from a truly personal genome viewpoint.
- Published in:
- Human Genetics, 2016, v. 135, n. 6, p. 591, doi. 10.1007/s00439-016-1682-6
- By:
- Publication type:
- Article