Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations / / edited by Ali Samadikuchaksaraei and Morteza Seifi.
Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for development of many human diseases. This book addresses the methods of detection, analysis, and interpretation of genomic variations in clinically relevant scenarios. If your research or clinical pra...
Saved in:
TeilnehmendeR: | |
---|---|
Place / Publishing House: | London, United Kingdom : : IntechOpen,, 2019. |
Year of Publication: | 2019 |
Language: | English |
Physical Description: | 1 online resource (100 pages) |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
LEADER | 02221nam a2200409 i 4500 | ||
---|---|---|---|
001 | 993548277904498 | ||
005 | 20240618145516.0 | ||
006 | m o d | ||
007 | cr#||||||||||| | ||
008 | 221006s2019 enk o 000 0 eng d | ||
020 | |a 1-83881-844-8 | ||
020 | |a 1-78923-800-5 | ||
035 | |a (CKB)4100000009913373 | ||
035 | |a (NjHacI)994100000009913373 | ||
035 | |a (oapen)https://directory.doabooks.org/handle/20.500.12854/66994 | ||
035 | |a (EXLCZ)994100000009913373 | ||
040 | |a NjHacI |b eng |e rda |c NjHacl | ||
041 | 0 | |a eng | |
050 | 4 | |a R724 |b .B565 2019 | |
082 | 0 | 4 | |a 174.2 |
100 | 1 | |a Samadikuchaksaraei, Ali |4 edt | |
245 | 0 | 0 | |a Bioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations / |c edited by Ali Samadikuchaksaraei and Morteza Seifi. |
260 | |b IntechOpen |c 2019 | ||
264 | 1 | |a London, United Kingdom : |b IntechOpen, |c 2019. | |
300 | |a 1 online resource (100 pages) | ||
336 | |a text |b txt |2 rdacontent | ||
337 | |a computer |b c |2 rdamedia | ||
338 | |a online resource |b cr |2 rdacarrier | ||
588 | |a Description based on publisher supplied metadata and other sources. | ||
506 | |a Open access |f Unrestricted online access |2 star | ||
520 | |a Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for development of many human diseases. This book addresses the methods of detection, analysis, and interpretation of genomic variations in clinically relevant scenarios. If your research or clinical practice involves handling of genomic sequencing data, this book is for you. Topics covered include: methods for identifying genetic diversity, the workflow for analyzing whole exome and whole genome sequencing data, local ancestry deconvolution models, the value of molecular patterns and pattern biomarkers in cancer diagnosis and prognosis, and genotyping and profiling resistance-associated variants of hepatitis C. If your research or clinical practice involves handling of genomic sequencing data, this book is for you. | ||
546 | |a English | ||
650 | 0 | |a Medical ethics. | |
653 | |a Medical bioinformatics | ||
776 | |z 1-78923-799-8 | ||
700 | 1 | |a Seifi, Morteza, |e editor. | |
700 | 1 | |a Samadikuchaksaraei, Ali, |e editor. | |
906 | |a BOOK | ||
ADM | |b 2024-06-19 06:42:33 Europe/Vienna |f system |c marc21 |a 2019-12-08 04:53:41 Europe/Vienna |g false | ||
AVE | |i DOAB Directory of Open Access Books |P DOAB Directory of Open Access Books |x https://eu02.alma.exlibrisgroup.com/view/uresolver/43ACC_OEAW/openurl?u.ignore_date_coverage=true&portfolio_pid=5338805920004498&Force_direct=true |Z 5338805920004498 |b Available |8 5338805920004498 |