Otros materiales y recursos sobre las tecnolog\u00edas \u00f3micas est\u00e1n a su disposici\u00f3n aqu\u00ed.<\/p>\n
BOLET\u00cdN GenoMed:<\/strong><\/p>\n En formato PDF, editado por la C\u00e1tedra Multidisciplinaria de Medicina Gen\u00f3mica, de la Universidad de Ciencias M\u00e9dicas de Las Tunas<\/a>.<\/p>\n – A\u00f1o 2019;1(2).<\/strong><\/a><\/p>\n – A\u00f1o 2019;1(1).<\/strong><\/a><\/p>\n <\/p>\n SUPERCURSOS:<\/strong><\/p>\n – Introducci\u00f3n a la Bioinform\u00e1tica<\/strong><\/a>. En formato .ppt, la descarga redirige al sitio de la Universidad Virtual de la Salud<\/a> de Cuba.<\/p>\n – Bioinformatics<\/a><\/strong>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Bioinformatics II<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Finishing the Human Genome<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Bias in Studies of the Human Genome<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Genome Databases<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Genome Databases – 2<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Genome-Wide Association Studies: Linking Genes to Disease. Part I<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Genome-Wide Association Studies: Linking Genes to Disease. Part II<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Genomics and Bioinformatics<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Genomics Bioinformatics & Medicine<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Human Genome Project. Part I<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Human Genome Project. Part II<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Next Generation Sequencing and Human Genome Databases<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Personal Genomics<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Pharmacogenomics<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Sequencing the Human Genome<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n – Sequence Alignment<\/strong><\/a>. WHO Collaborating Center University of Pittsburgh.<\/p>\n <\/p>\n CURSOS EN L\u00cdNEA:<\/strong><\/p>\n – El Proyecto Genoma Humano, 10 a\u00f1os despu\u00e9s: mitos y realidades<\/strong><\/a>. Instituto Roche, Espa\u00f1a. Celebrado los d\u00edas 8 y 9 de abril de 2011. Presentaciones contienen audio<\/strong>.<\/p>\n – Bioinform\u00e1tica y an\u00e1lisis gen\u00f3micos en el estudio de enfermedades raras<\/strong><\/a>. Conferencia dictada por Joaqu\u00edn Dopazo, Director de Gen\u00f3mica Funcional, Centro de Investigaci\u00f3n Pr\u00edncipe Felipe, Valencia, Espa\u00f1a. Hospedado por Instituto Roche, Espa\u00f1a. Presentaci\u00f3n contiene audio<\/strong>.<\/p>\n – The Human Genome: A Decade of Discovery, Creating a Healthy Future<\/strong><\/a>. NHGRI, EEUU. Junio 7, 2010.<\/p>\n – Understanding the Human Genome Project<\/strong><\/a>. NHGRI, EEUU. Noviembre 24, 2010.<\/p>\n – The Human Genome Project and Beyond<\/strong><\/a>. US Department of Energy. Junio 2008.<\/p>\n – Gen\u00f3mica y Prote\u00f3mica en Cl\u00ednica<\/strong><\/a>. Instituto Roche, Espa\u00f1a. 27 de noviembre de 2007.<\/p>\n – Genome-Wide Association Studies for the Rest of Us: Adding Genome-Wide Association to Population Studies<\/strong><\/a>. Boston, Mass., EEUU. Junio 22, 2007.<\/p>\n <\/p>\n COLECCIONES Y OTROS:<\/strong><\/p>\n – Microbiota intestinal<\/strong><\/a>. Nature Outlook January, 2020.<\/p>\n – CRISPR\/Cas Collection<\/a><\/strong>. Nucleic Acids Research, 2016.<\/p>\n – Precision Cancer Medicine<\/strong><\/a>. Genome Medicine special issue, November 2016.<\/p>\n – Precision medicine<\/strong><\/a>. Nature 2016;537(7619_supp):S49-S96.<\/p>\n – The Biology of Human Diseases, as Revealed Through Genomics<\/strong><\/a>. Genome Biology November-December 2016.<\/p>\n – Genome Editing in Haematology<\/strong><\/a>. The Blood Journal, Review Series May 26, 2016.<\/p>\n – Pharmacogenetics<\/strong><\/a>. JAMA Collections, 2015.<\/p>\n – Single-Cell Omics<\/strong><\/a>. Genome Biology.<\/p>\n – Genome editing<\/strong><\/a>. Genome Biology.<\/p>\n – Immunogenomics in health and disease<\/strong><\/a>. Colecci\u00f3n de Genome Medicine.<\/p>\n – Single-cell omics<\/strong><\/a>. Serie de Nature Genetics Reviews.<\/p>\n – Single Cell Genomics<\/strong><\/a>. PLOS ONE 2015.<\/p>\n – Precision Medicine Initiative<\/strong><\/a>.\u00a0 P\u00e1gina informativa en sitio de Institutos Nacionales de Salud.<\/p>\n – Genome editing<\/strong><\/a>. Nature Outlook 2015;528(7580_supp):S1-S48.<\/p>\n – Big data in biomedicine<\/strong><\/a>. Special Nature 2015;527(7576_supp):S1-S19.<\/p>\n – Computational biology and bioinformatics<\/strong><\/a>. Nature subject area.<\/p>\n – The 1000 Genomes Project<\/strong><\/a>. Nature Collection, 2015. Nature Publishing Group.<\/p>\n – Genomics of infectious diseases special issue<\/strong><\/a>. BioMedCentral. Published: 3 November 2014. Last updated: 17 February 2015.<\/p>\n – Applications of next-generation sequencing<\/strong><\/a>. Nature, 2009 – 2015.<\/p>\n – Computational Tools<\/strong><\/a>.\u00a0 Nature, 2010 – 2014.<\/p>\n – Clinical applications of next-generation sequencing<\/strong><\/a>. Nature, 2013.<\/p>\n – Participatory Medicine<\/strong><\/a>. Genome Medicine, 20 December 2013.<\/p>\n – Cancer bioinformatics: bioinformatic methods, network biomarkers and precision medicine<\/strong><\/a>. BioMedCentral, 1 May 2012. Actualizado: 26 November 2012.<\/p>\n – The Human Genome at Ten<\/strong><\/a>. Nature, 2011.<\/p>\n – Milestones in DNA Technologies<\/strong><\/a>. Nature, 2011.<\/p>\n – Human Genome Resources<\/strong><\/a>. NCBI.<\/p>\n – Genomes and Disease<\/strong><\/a>. Nature, 2010.<\/p>\n – The ‘Omics Age<\/strong><\/a>. Nature, 2010.<\/p>\n – Genomics<\/strong><\/a>. Nature, 2010.<\/p>\n – The Human Genome Project<\/strong><\/a>. Nature, 2010.<\/p>\n – Genomics of Emerging Infectious Diseases<\/strong><\/a>. PLOS Biology 2009.<\/p>\n – Prokaryotic Genome Collection<\/strong><\/a>. PLOS ONE 2009.<\/p>\n – Education<\/strong><\/a>. PLOS Computational Biology, 2006.<\/p>\n – Nature issue 15 February 2001<\/strong><\/a> (the human genome)<\/p>\n REGULACIONES:<\/strong><\/p>\n – Raca G, Astbury C, Behlmann A, de Castro MJ, Hickey SE, Karaca E, et al. Points to consider in the detection of germline structural variants using next-generation sequencing: A statement of the American College of Medical Genetics and Genomics (ACMG)<\/strong><\/a>. Genetics in Medicine, 2022; https:\/\/doi.org\/10.1016\/j.gim.2022.09.017.<\/p>\n – Murray MF, Giovanni MA, Doyle DL, Harrison SM, Lyon E, Manickam K, et al. DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG)<\/a><\/strong>. Genetics in Medicine 2021; https:\/\/doi.org\/10.1038\/s41436-020-01082-w.<\/p>\n – Monaghan KG, Leach NT, Pekarek D, Prasad P, Rose NC, ACMG Professional Practice and Guidelines Committee. The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG)<\/a><\/strong>. Genetics in Medicine 2020; DOI: 10.1038\/s41436-019-0731-7.<\/p>\n – Rajagopal PS, Nielsen S, Olopade OI. USPSTF Recommendations for BRCA1 and BRCA2 Testing in the Context of a Transformative National Cancer Control Plan<\/a><\/strong>. JAMA Netw Open. 2019;2(8):e1910142.<\/p>\n – ACMG Board of Directors. The use of ACMG secondary findings recommendations for general population screening: a policy statement of the American College of Medical Genetics and Genomics (ACMG)<\/a><\/strong>. Genetics in Medicine 2019;21(1467\u20131468).<\/p>\n – Bombard Y, Brothers KB, Fitzgerald-Butt S, Garrison NA, Jamal L, James CA, et al<\/em>.\u00a0The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results<\/strong><\/a>. Am J Hum Gen 2019; DOI: https:\/\/doi.org\/10.1016\/j.ajhg.2019.02.025.<\/p>\n – Bartley AN, Washington MK, Colasacco C, Ventura CB, Ismaila N, Benson AB, et al<\/em>. HER2 Testing and Clinical Decision Making in Gastroesophageal Adenocarcinoma: Guideline From the College of American Pathologists, American Society for Clinical Pathology, and the American Society of Clinical Oncology<\/strong><\/a>. Journal of Clinical Oncology 2016; doi: 10.1200\/JCO.2016.69.4836.<\/p>\n – Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam MP, Belmont J, et al<\/em>. Recommendations for the integration of genomics into clinical practice<\/strong><\/a>. Genetics in Medicine 2016;18:1075\u20131084.<\/p>\n – Kleinberger J, Maloney KA, Pollin TI, Bone LJ. An openly available online tool for implementing the ACMG\/AMP standards and guidelines for the interpretation of sequence variants<\/strong><\/a>. Genetics in Medicine 2016;18:1165.<\/p>\n – Gregg AR, Skotko BG, Benkendorf JL, Monaghan KG, Bajaj K, Best RG, et al<\/em>. Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics<\/strong><\/a>. Genetics in Medicine 2016;18:1056\u20131065.<\/p>\n – Kalia SS, Adelman K, Bale SJ, Chung WK, Eng C, Evans JP, et al<\/em>. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics<\/strong><\/a>. Genetics in Medicine 2016; doi:10.1038\/gim.2016.190.<\/p>\n – Hunter JE, Irving SA, Biesecker LG, Buchanan A, Jensen B, Lee K, et al<\/em>. A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation<\/strong><\/a>. Genetics in Medicine 2016;18:1258\u20131268.<\/p>\n – Petrone J. FDA wades into sequencing-based diagnostics regulation<\/strong><\/a>. Nature Biotechnology 2016;34:681\u2013682.<\/p>\n – Altman RB, Prabhu S, Sidow A, Zook JM, Goldfeder R, Litwack D, et al<\/em>. A research roadmap for next-generation sequencing informatics<\/strong><\/a>. Science Translational Medicine\u00a0 20 Apr 2016;8(335):335ps10.<\/p>\n – ACMG Board of Directors. Direct-to-consumer genetic testing: a revised position statement of the American College of Medical Genetics and Genomics<\/strong><\/a>.\u00a0 Genetics in Medicine 2016;18:207\u2013208.<\/p>\n