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Dr Venkateswara Addala
Dr

Venkateswara Addala

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Overview

Background

Research officer, Medical Genomics

QIMR Berghofer Medical Research Institute

Availability

Dr Venkateswara Addala is:
Available for supervision

Research impacts

My research addressed the challenges related to key genomic components in tumour-immune editing variation in cancers with poor survival and predicting the responses to cancer immunotherapies. Characterizing genomic determinants in underlying response and resistance to cancer immunotherapy. Through whole genome and RNA sequencing, we identify tumor specific neoantigens that can elicit T-cell responses in cancers. Through established Immunogenomics analysis on different cancer types, we aim to explore the genomics of tumor cells and the properties of immune cells in the tumour microenvironment. Through further research, we uncover how tumours may prevent immune attack and why. We seek to better understand the tumour microenvironment and how it may contribute towards tumour growth. Lastly, we can uncover new techniques in patients screening to see who would benefit most from immunotherapies during the treatment of their disease.

In my PhD I established cancer immunogenomics analysis pipeline, to understand tumour heterogeneity in intrinsic and extrinsic mechanisms across cancer types. This work extends knowledge and lays the foundation that is required in order to successfully establish computational methods that can be used to predict patient immunotherapy responses to immune checkpoint inhibitors.

Works

Search Professor Venkateswara Addala’s works on UQ eSpace

25 works between 2013 and 2025

21 - 25 of 25 works

2020

Journal Article

Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity

Newell, Felicity, Wilmott, James S., Johansson, Peter A., Nones, Katia, Addala, Venkateswar, Mukhopadhyay, Pamela, Broit, Natasa, Amato, Carol M., Van Gulick, Robert, Kazakoff, Stephen H., Patch, Ann-Marie, Koufariotis, Lambros T., Lakis, Vanessa, Leonard, Conrad, Wood, Scott, Holmes, Oliver, Xu, Qinying, Lewis, Karl, Medina, Theresa, Gonzalez, Rene, Saw, Robyn P. M., Spillane, Andrew J., Stretch, Jonathan R., Rawson, Robert V., Ferguson, Peter M., Dodds, Tristan J., Thompson, John F., Long, Georgina V., Levesque, Mitchell P. ... Hayward, Nicholas K. (2020). Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity. Nature Communications, 11 (1) 5259, 5259. doi: 10.1038/s41467-020-18988-3

Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity

2018

Journal Article

Apert's syndrome: study by whole exome sequencing

Munshi, Anjana, Khetarpal, Preeti, Das, Satrupa, Rao, Venkateshwar, Valecha, Monica, Bansal, Manita and Kumar, Roshan (2018). Apert's syndrome: study by whole exome sequencing. Genes and Diseases, 5 (2), 119-122. doi: 10.1016/j.gendis.2017.07.008

Apert's syndrome: study by whole exome sequencing

2018

Journal Article

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

Patch, Ann-Marie, Nones, Katia, Kazakoff, Stephen H., Newell, Felicity, Wood, Scott, Leonard, Conrad, Holmes, Oliver, Xu, Qinying, Addala, Venkateswar, Creaney, Jenette, Robinson, Bruce W., Fu, Shujin, Geng, Chunyu, Li, Tong, Zhang, Wenwei, Liang, Xinming, Rao, Junhua, Wang, Jiahao, Tian, Mingyu, Zhao, Yonggang, Teng, Fei, Gou, Honglan, Yang, Bicheng, Jiang, Hui, Mu, Feng, Pearson, John V. and Waddell, Nicola (2018). Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing. PloS One, 13 (1) e0190264, e0190264. doi: 10.1371/journal.pone.0190264

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

2017

Journal Article

Identification of unique neoantigen qualities in long-term survivors of pancreatic cancer

Balachandran, Vinod P., Łuksza, Marta, Zhao, Julia N., Makarov, Vladimir, Moral, John Alec, Remark, Romain, Herbst, Brian, Askan, Gokce, Bhanot, Umesh, Senbabaoglu, Yasin, Wells, Daniel K., Cary, Charles Ian Ormsby, Grbovic-Huezo, Olivera, Attiyeh, Marc, Medina, Benjamin, Zhang, Jennifer, Loo, Jennifer, Saglimbeni, Joseph, Abu-Akeel, Mohsen, Zappasodi, Roberta, Riaz, Nadeem, Smoragiewicz, Martin, Larkin Kelley, Z., Basturk, Olca, Gönen, Mithat, Levine, Arnold J., Allen, Peter J., Fearon, Douglas T., Merad, Miriam ... Bassi, Claudio (2017). Identification of unique neoantigen qualities in long-term survivors of pancreatic cancer. Nature, 551 (7681), 512-516. doi: 10.1038/nature24462

Identification of unique neoantigen qualities in long-term survivors of pancreatic cancer

2013

Journal Article

Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients

Dadheech, Sneha, Rao, A. Venkateswara, Shaheen, Uzma, Hussien, Mohammed Dyia, Jain, Suman, Jyothy, A. and Munshi, Anjana (2013). Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients. Gene, 531 (2), 301-5. doi: 10.1016/j.gene.2013.08.078

Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients

Supervision

Availability

Dr Venkateswara Addala is:
Available for supervision

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Supervision history

Current supervision

Media

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