{"product_id":"9780081019610","title":"Statistics for Bioinformatics: Methods for Multiple Sequence Alignment","description":"\u003cp\u003e\u003ci\u003eStatistics for Bioinformatics: Methods for Multiple Sequence Alignment\u003c\/i\u003e provides an in-depth introduction to the most widely used methods and software in the bioinformatics field. With the ever increasing flood of sequence information from genome sequencing projects, multiple sequence alignment has become one of the cornerstones of bioinformatics. Multiple sequence alignments are crucial for genome annotation, as well as the subsequent structural, functional, and evolutionary studies of genes and gene products. Consequently, there has been renewed interest in the development of novel multiple sequence alignment algorithms and more efficient programs. \u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eExplains the dynamics that animate health systems\u003c\/li\u003e\n\u003cli\u003eExplores tracks to build sustainable and equal architecture of health systems\u003c\/li\u003e\n\u003cli\u003eExamines the advantages and disadvantages of the different approaches to care integration and the management of health information\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Elsevier Science","offers":[{"title":"Default Title","offer_id":47079420395760,"sku":"9780081019610","price":80.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0737\/7593\/9824\/files\/9780081019610_p0.jpg?v=1763638443","url":"https:\/\/shop-qa.barnesandnoble.com\/products\/9780081019610","provider":"Barnes \u0026 Noble (DEV)","version":"1.0","type":"link"}