Children’s rare disease cohorts: an integrative research and clinical genomics initiative

While genomic data is frequently collected under distinct research protocols and disparate clinical and research regimes, there is a benefit in streamlining sequencing strategies to create harmonized databases, particularly in the area of pediatric rare disease. Research hospitals seeking to impleme...

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Veröffentlicht in:	Npj genomic medicine 2020-07, Vol.5 (1), p.29-29, Article 29
Hauptverfasser:	Rockowitz, Shira, LeCompte, Nicholas, Carmack, Mary, Quitadamo, Andrew, Wang, Lily, Park, Meredith, Knight, Devon, Sexton, Emma, Smith, Lacey, Sheidley, Beth, Field, Michael, Holm, Ingrid A., Brownstein, Catherine A., Agrawal, Pankaj B., Kornetsky, Susan, Poduri, Annapurna, Snapper, Scott B., Beggs, Alan H., Yu, Timothy W., Williams, David A., Sliz, Piotr
Format:	Artikel
Sprache:	eng
Schlagworte:	631/114/129/2043 631/114/1314 631/208/212/2166 631/208/212/2301 692/700/1720 Bioinformatics Biomedical and Life Sciences Biomedicine Gene Function Gene Therapy Genomics Human Genetics Internal Medicine Pediatrics Rare diseases
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