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Functional & Integrative GenomicsGenomicsPeer-reviewed journal article

MyeloDB: A multi-omics resource for Multiple Myeloma

Ambuj KumariD, Keerthana Vinod Kumar, Kavita KundaliD, Avik SenguptaiD, Simran SharmaiD, R Kunjulakshmi, Rahul KumariD

PDFDOIPreprint

Abstract

Multiple myeloma (MM) is a common type of blood cancer affecting plasma cells originating from the lymphoid B-cell lineage. It accounts for about 10% of all haematological malignancies and can cause significant end-organ damage. The emergence of genomic technologies such as next-generation sequencing and gene expression analysis has opened new possibilities for early detection of multiple myeloma and identification of personalized treatment options. However, there remain significant challenges to overcome in MM research, including integrating multi-omics data, achieving a comprehensive understanding of the disease, and developing targeted therapies and biomarkers. The extensive data generated by these technologies presents another challenge for data analysis and interpretation. To bridge this gap, we have developed a multi-omics open-access database called MyeloDB. It includes gene expression profiling, high throughput CRISPR-Cas9 screens, drug sensitivity resources profile, and biomarkers. MyeloDB contains 47 expression profiles, 3 methylation profiles comprising a total of 5630 patient samples and 15 biomarkers which were reported in previous studies. In addition to this, MyeloDB can provide significant insight of gene mutations in MM on drug sensitivity. Furthermore, users can download the datasets and conduct their own analyses. Utilizing this database, we have identified five novel genes i.e., CBFB, MANF, MBNL1, SEPHS2 and UFM1 as potential drug targets for MM. We hope MyeloDB will serve as a comprehensive platform for researchers and foster novel discoveries in MM. MyeloDB is freely accessible at: (https://project.iith.ac.in/cgntlab/myelodb/)

Citations
4
FWCI
1.24
Field percentile
top 22%

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Keerthana Vinod Kumar, Ambuj Kumar, Kavita Kundal+4 more·bioRxiv·May 19, 2023· 1 citations