ALEKSANDAR MILOSAVLJEVIC to Software
This is a "connection" page, showing publications ALEKSANDAR MILOSAVLJEVIC has written about Software.
Connection Strength
3.244
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ClinGen API platform for classification of human genetic variants. Cell Genom. 2026 Apr 08; 6(4):101211.
Score: 0.666
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The NanoFlow Repository. Bioinformatics. 2023 06 01; 39(6).
Score: 0.546
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Analysis of interactions between the epigenome and structural mutability of the genome using Genboree Workbench tools. BMC Bioinformatics. 2014; 15 Suppl 7:S2.
Score: 0.293
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ReadDepth: a parallel R package for detecting copy number alterations from short sequencing reads. PLoS One. 2011 Jan 31; 6(1):e16327.
Score: 0.232
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Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing. BMC Bioinformatics. 2010 Nov 23; 11:572.
Score: 0.229
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Pash 2.0: scaleable sequence anchoring for next-generation sequencing technologies. Pac Symp Biocomput. 2008; 102-13.
Score: 0.188
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Aggregation of gene regulatory information and knowledge on FAIR principles enables discovery of pathogenic gene regulatory variants. Bioinformatics. 2026 Feb 28; 42(3).
Score: 0.165
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Playbook workflow builder: Interactive construction of bioinformatics workflows. PLoS Comput Biol. 2025 Apr; 21(4):e1012901.
Score: 0.155
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Pash: efficient genome-scale sequence anchoring by Positional Hashing. Genome Res. 2004 Apr; 14(4):672-8.
Score: 0.145
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exRNA Atlas Analysis Reveals Distinct Extracellular RNA Cargo Types and Their Carriers Present across Human Biofluids. Cell. 2019 04 04; 177(2):463-477.e15.
Score: 0.102
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exceRpt: A Comprehensive Analytic Platform for Extracellular RNA Profiling. Cell Syst. 2019 04 24; 8(4):352-357.e3.
Score: 0.102
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ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants. Genome Med. 2017 01 12; 9(1):3.
Score: 0.088
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Atlas2 Cloud: a framework for personal genome analysis in the cloud. BMC Genomics. 2012; 13 Suppl 6:S19.
Score: 0.066
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The Genboree Microbiome Toolset and the analysis of 16S rRNA microbial sequences. BMC Bioinformatics. 2012; 13 Suppl 13:S11.
Score: 0.065
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An integrative variant analysis suite for whole exome next-generation sequencing data. BMC Bioinformatics. 2012 Jan 12; 13:8.
Score: 0.062
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MPAPASS software enables stitched multiplex, multidimensional EV repertoire analysis and a standard framework for reporting bead-based assays. Cell Rep Methods. 2022 01 24; 2(1):100136.
Score: 0.031
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Guidelines for cell-type heterogeneity quantification based on a comparative analysis of reference-free DNA methylation deconvolution software. BMC Bioinformatics. 2020 Jan 13; 21(1):16.
Score: 0.027
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ClinGen Allele Registry links information about genetic variants. Hum Mutat. 2018 11; 39(11):1690-1701.
Score: 0.025
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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: 0.021
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DNA sequence recognition by hybridization to short oligomers. J Comput Biol. 1995; 2(2):355-70.
Score: 0.019
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Prototypic sequences for human repetitive DNA. J Mol Evol. 1992 Oct; 35(4):286-91.
Score: 0.016