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Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.

, , , , , , , and . Nucleic Acids Res., 32 (Database-Issue): 537-541 (2004)

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Systems Biology in Heterogenous Tissues: Integrating Multiple *Omics Datasets to Understand Hematopoietic Differentiation., , , , , , , and . BIBE, page 240-243. IEEE, (2019)ORegAnno: an open-access community-driven resource for regulatory annotation., , , , , , , , , and 19 other author(s). Nucleic Acids Res., 36 (Database-Issue): 107-113 (2008)The UCSC Genome Browser database: update 2010., , , , , , , , , and 13 other author(s). Nucleic Acids Res., 38 (Database-Issue): 613-619 (2010)Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations., , , , , , and . Nucleic Acids Res., 49 (Database-Issue): D1192-D1196 (2021)S3V2-IDEAS: a package for normalizing, denoising and integrating epigenomic datasets across different cell types., , , , and . Bioinform., 37 (18): 3011-3013 (2021)The UCSC Genome Browser database: update 2011., , , , , , , , , and 17 other author(s). Nucleic Acids Res., 39 (Database-Issue): 876-882 (2011)Updates of the HbVar database of human hemoglobin variants and thalassemia mutations., , , , , , , , , and 3 other author(s). Nucleic Acids Res., 42 (Database-Issue): 1063-1069 (2014)Improvements to GALA and dbERGE II: databases featuring genomic sequence alignment, annotation and experimental results., , , , , , , , and . Nucleic Acids Res., 33 (Database-Issue): 466-470 (2005)The UCSC Genome Browser database: extensions and updates 2013., , , , , , , , , and 22 other author(s). Nucleic Acids Res., 41 (Database-Issue): 64-69 (2013)Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies., , , , , , , and . Nucleic Acids Res., 32 (Database-Issue): 537-541 (2004)