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Biology subjects

Santander, C.

Publications and source records attributed to Santander, C..

2 recordsLinked to original sources

Multi-scale haplotype signatures distinguish among evolutionary processes

Natural selection embeds distinct genomic signatures as populations adapt to environmental pressures. Machine learning approaches, particularly deep neural networks, have emerged as powerful tools to detect adaptive signatures from genomic data. While machine learning has dramatically improved our ability to extract these signals from sequence variation, distinguishing among multiple evolutionary processes remains challenging. We introduce SHADES, a deep learning framework that employs information about sequence differences and their frequencies at various spatial resolutions to capture evolutionary signatures at different genomic scales. We found that SHADES has the capacity to distinguish among neutrality, selective sweeps, balancing selection, and adaptive introgression and outperformed several contemporary methods evaluated for both classification accuracy and power. In addition, SHADES remained robust to a number of confounding factors, with only modest changes in classification performance. Furthermore, application of SHADES to empirical haplotypic variation from European humans recovered previously reported signals for selective sweeps, balancing selection, and adaptive introgression, while also identifying novel genes broadly involved in immune defense, inflammatory regulation, and epithelial barrier biology.

genomics↗

Faster model-based estimation of ancestry proportions

Ancestry estimation from genotype data in unrelated individuals has become an essential tool in population and medical genetics to understand demographic population histories and to model or correct for population structure. The ADMIXTURE software is a widely used model-based approach to account for population stratification, however, it struggles with convergence issues and does not scale to modern human datasets or the large number of variants in whole-genome sequencing data. Likelihood-free approaches optimize a least square objective and have gained popularity in recent years due to their scalability. However, this comes at the cost of accuracy in the ancestry estimates in more complex admixture scenarios. We present a new model-based approach, fastmixture, which adopts aspects from likelihood-free approaches for parameter initialization, followed by a mini-batch expectation-maximization procedure to model the standard likelihood. In a simulation study, we demonstrate that the model-based approaches of fastmixture and ADMIXTURE are significantly more accurate than recent and likelihood-free approaches. We further show that fastmixture runs approximately 30x faster than ADMIXTURE on both simulated and empirical data from the 1000 Genomes Project such that our model-based approach scales to much larger sample sizes than previously possible. Our software is freely available at https://github.com/Rosemeis/fastmixture.

bioinformatics↗