ALEKSANDAR MILOSAVLJEVIC to Genomics
This is a "connection" page, showing publications ALEKSANDAR MILOSAVLJEVIC has written about Genomics.
Connection Strength
0.542
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ClinGen API platform for classification of human genetic variants. Cell Genom. 2026 Apr 08; 6(4):101211.
Score: 0.134
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Mapping MAVE data for use in human genomics applications. Genome Biol. 2025 Jun 25; 26(1):179.
Score: 0.127
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Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard. Appl Clin Inform. 2016 08 31; 7(3):817-31.
Score: 0.069
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Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium. Am J Hum Genet. 2016 06 02; 98(6):1067-1076.
Score: 0.068
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Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature. 2004 04 01; 428(6982):493-521.
Score: 0.029
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The EN-TEx resource of multi-tissue personal epigenomes?& variant-impact models. Cell. 2023 03 30; 186(7):1493-1511.e40.
Score: 0.027
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tmVar 3.0: an improved variant concept recognition and normalization tool. Bioinformatics. 2022 09 15; 38(18):4449-4451.
Score: 0.026
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ClinGen advancing genomic data-sharing standards as a GA4GH driver project. Hum Mutat. 2018 11; 39(11):1686-1689.
Score: 0.020
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Comparison and quantitative verification of mapping algorithms for whole-genome bisulfite sequencing. Nucleic Acids Res. 2014 Apr; 42(6):e43.
Score: 0.014
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ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia. Genome Res. 2012 Sep; 22(9):1813-31.
Score: 0.013
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An integrative variant analysis suite for whole exome next-generation sequencing data. BMC Bioinformatics. 2012 Jan 12; 13:8.
Score: 0.013