bioRxiv Science⌕ Search

Biology subjects

Cosgun, E.

Publications and source records attributed to Cosgun, E..

2 recordsLinked to original sources

Boosting GPT Models for Genomics Analysis: Generating Trusted Genetic Variant Annotations and Interpretations through RAG and fine-tuning

Large language models (LLMs) have acquired a remarkable level of knowledge through their initial training. However, they lack expertise in particular domains such as genomics. Variant annotation data, an important component of genomics, is crucial for interpreting and prioritizing disease-related variants among millions of variants identified by genetic sequencing. In our project, we aimed to improve LLM performance in genomics by adding variant annotation data to LLMs by retrieval-augmented generation (RAG) and fine-tuning techniques. Using RAG, we successfully integrated 190 million highly accurate variant annotations, curated from 5 major annotation datasets and tools, into GPT-4o. This integration empowers users to query specific variants and receive accurate variant annotations and interpretations supported by advanced reasoning and language understanding capabilities of LLMs. Additionally, fine-tuning GPT-4 on variant annotation data also improved model performance in some annotation fields, although the accuracy across more fields remains suboptimal. Our model significantly improved the accessibility and efficiency of the variant interpretation process by leveraging LLM capabilities. Our project also revealed that RAG outperforms fine-tuning in factual knowledge injection in terms of data volume, accuracy, and cost-effectiveness. As a pioneering study for adding genomics knowledge to LLMs, our work paves the way for developing more comprehensive and informative genomics AI systems to support clinical diagnosis and research projects, and it demonstrates the potential of LLMs in specialized domains.

genetics↗

Prediction of Polygenic Risk Score by Machine Learning and Deep Learning Methods in Genome-wide Association Studies

Polygenic risk score (PRS) is a method that using multiple SNPs simultaneously and can be calculated as a typical disease risk score. It is useful method for precision and personalised medicine. Calculating PRS with the classical method, it is frequently used to use two different data sets which are training and testing sets. It is a disadvantage for the classical method. By using a single data set, machine learning (ML) and deep learning (DL) methods both avoid the problem of overfitting and can be used as a good alternative method. Genome-wide Association Studies (GWAS) data were generated with the PLINK Program by replicating a hundred times at different allele frequencies and different sample size. We applied two different ML algorithms which are Support Vector Machine (SVM) and Random Forest (RF) as well as DL approach. ML methods can obtain more consistent results in terms of case-control separation compared to PRS calculated with the classical method (PRS). The use of ML and DL methods as an alternative to classical methods to calculate PRS has been suggested.

bioinformatics↗