000			02163naaaa2200337uu 4500
001			https://directory.doabooks.org/handle/20.500.12854/66994
005			20220219213914.0
020			_aintechopen.77443
020			_a9781789238006
020			_a9781789237993
020			_a9781838818449
024	7		_a10.5772/intechopen.77443 _cdoi
041	0		_aEnglish
042			_adc
072		7	_aMBDC _2bicssc
100	1		_aSamadikuchaksaraei, Ali _4edt
700	1		_aSeifi, Morteza _4edt
700	1		_aSamadikuchaksaraei, Ali _4oth
700	1		_aSeifi, Morteza _4oth
245	1	0	_aBioinformatics Tools for Detection and Clinical Interpretation of Genomic Variations
260			_bIntechOpen _c2019
300			_a1 electronic resource (100 p.)
506	0		_aOpen Access _2star _fUnrestricted online access
520			_aGenomic 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.
540			_aCreative Commons _fhttps://creativecommons.org/licenses/by/3.0/ _2cc _4https://creativecommons.org/licenses/by/3.0/
546			_aEnglish
650		7	_aMedical ethics & professional conduct _2bicssc
653			_aMedical bioinformatics
856	4	0	_awww.oapen.org _uhttps://mts.intechopen.com/storage/books/7639/authors_book/authors_book.pdf _70 _zDOAB: download the publication
856	4	0	_awww.oapen.org _uhttps://directory.doabooks.org/handle/20.500.12854/66994 _70 _zDOAB: description of the publication
999			_c45459 _d45459