Aleksandar Mihajlović

ORCID: 0009-0003-9122-229X
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About
Contact & Profiles
Research Areas
  • Cancer Genomics and Diagnostics
  • Gene expression and cancer classification
  • Bioinformatics and Genomic Networks
  • Genetics, Bioinformatics, and Biomedical Research
  • Single-cell and spatial transcriptomics
  • Scientific Computing and Data Management
  • Research Data Management Practices
  • Algorithms and Data Compression
  • Genomics and Phylogenetic Studies
  • Molecular Biology Techniques and Applications
  • Cell Image Analysis Techniques
  • Genetic Associations and Epidemiology
  • 3D Surveying and Cultural Heritage
  • Image Processing and 3D Reconstruction

Seven Bridges Genomics (United States)
2017

Mathematical Institute of the Serbian Academy of Sciences and Arts
2013-2014

Serbian Academy of Sciences and Arts
2013-2014

The Seven Bridges Cancer Genomics Cloud (CGC; www.cancergenomicscloud.org) enables researchers to rapidly access and collaborate on massive public cancer genomic datasets, including Genome Atlas. It provides secure on-demand data, analysis tools, computing resources. Researchers from diverse backgrounds can easily visualize, query, explore datasets visually or programmatically. Data of interest be immediately analyzed in the cloud using more than 200 preinstalled, curated bioinformatics...

10.1158/0008-5472.can-17-0387 article EN Cancer Research 2017-10-31

The Playbook Workflow Builder (PWB) is a web-based platform to dynamically construct and execute bioinformatics workflows by utilizing growing network of input datasets, semantically annotated API endpoints, data visualization tools contributed an ecosystem collaborators. Via user-friendly user interface, can be constructed from building-blocks without technical expertise. output each step the workflow added into reports containing textual descriptions, figures, tables, references. To...

10.1371/journal.pcbi.1012901 article EN cc-by PLoS Computational Biology 2025-04-03

Abstract Many biomedical research projects produce large-scale datasets that may serve as resources for the community hypothesis generation, facilitating diverse use cases. Towards goal of developing infrastructure to support findability, accessibility, interoperability, and reusability (FAIR) digital objects maximally extracting knowledge from data, complex queries span across data tools multiple are currently not easily possible. By utilizing existing FAIR application programming...

10.1101/2024.06.08.598037 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2024-06-09

<div>Abstract<p>The Seven Bridges Cancer Genomics Cloud (CGC; <a href="http://www.cancergenomicscloud.org" target="_blank">www.cancergenomicscloud.org</a>) enables researchers to rapidly access and collaborate on massive public cancer genomic datasets, including The Genome Atlas. It provides secure on-demand data, analysis tools, computing resources. Researchers from diverse backgrounds can easily visualize, query, explore datasets visually or programmatically. Data...

10.1158/0008-5472.c.7360326.v1 preprint EN 2024-07-22

<p>Video 1. Narrated screencast highlighting the major features of CGC. For additional videos, tutorials and user guides, visit knowledge center (<a href="http://docs.cancergenomicscloud.org" target="_blank">docs.cancergenomicscloud.org</a>)</p>

10.1158/0008-5472.26349423.v1 preprint EN 2024-07-22

<p>Video 1. Narrated screencast highlighting the major features of CGC. For additional videos, tutorials and user guides, visit knowledge center (<a href="http://docs.cancergenomicscloud.org" target="_blank">docs.cancergenomicscloud.org</a>)</p>

10.1158/0008-5472.26349423 preprint EN 2024-07-22

<div>Abstract<p>The Seven Bridges Cancer Genomics Cloud (CGC; <a href="http://www.cancergenomicscloud.org" target="_blank">www.cancergenomicscloud.org</a>) enables researchers to rapidly access and collaborate on massive public cancer genomic datasets, including The Genome Atlas. It provides secure on-demand data, analysis tools, computing resources. Researchers from diverse backgrounds can easily visualize, query, explore datasets visually or programmatically. Data...

10.1158/0008-5472.c.7360326 preprint EN 2024-07-22

<div>Abstract<p>The Seven Bridges Cancer Genomics Cloud (CGC; <a href="http://www.cancergenomicscloud.org" target="_blank">www.cancergenomicscloud.org</a>) enables researchers to rapidly access and collaborate on massive public cancer genomic datasets, including The Genome Atlas. It provides secure on-demand data, analysis tools, computing resources. Researchers from diverse backgrounds can easily visualize, query, explore datasets visually or programmatically. Data...

10.1158/0008-5472.c.7360326.v2 preprint EN 2024-07-24

<p>Video 1. Narrated screencast highlighting the major features of CGC. For additional videos, tutorials and user guides, visit knowledge center (<a href="http://docs.cancergenomicscloud.org" target="_blank">docs.cancergenomicscloud.org</a>)</p>

10.1158/0008-5472.26367166 preprint EN cc-by 2024-07-24

<p>Video 1. Narrated screencast highlighting the major features of CGC. For additional videos, tutorials and user guides, visit knowledge center (<a href="http://docs.cancergenomicscloud.org" target="_blank">docs.cancergenomicscloud.org</a>)</p>

10.1158/0008-5472.26367166.v1 preprint EN 2024-07-24

Single-cell DNA sequencing is a powerful tool to evaluate the state of heterogeneity heterogeneous tissues like cancer in quantitative manner that bulk can never achieve. DOP-PCR (Degenerate Oligonucleotide-Primed Polymerase Chain Reaction), MDA (Multiple Displacement Amplification), MALBAC Annealing and Looping-Based Amplification Cycles), LIANTI (Linear via Transposon Insertion) TnBC (Transposon Barcoded) have been primary choices prepare single-cell libraries. library prep method simple...

10.21769/bioprotoc.3175 article EN BIO-PROTOCOL 2019-01-01

Single-cell sequencing provides a new level of granularity in studying the heterogeneous nature cancer cells. For some cancers, this heterogeneity is result copy number changes genes within cellular genomes. The ability to accurately determine such critical tracing and understanding tumorigenesis. Current single-cell genome methodologies infer numbers based on statistical approaches followed by rounding decimal integer values. Such are sample dependent, have varying calling sensitivities...

10.1038/s41598-021-97852-w article EN cc-by Scientific Reports 2021-09-23
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