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1. ILS-Aware Analysis of Low-Homoplasy Retroelement Insertions: Inference of Species Trees and Introgression Using Quartets

   https://doi.org/10.1093/jhered/esz076  

   Springer, Mark S; Molloy, Erin K; Sloan, Daniel B; Simmons, Mark P; Gatesy, John (December 2019, Journal of Heredity)

   Murphy, William (Ed.)

   Abstract DNA sequence alignments have provided the majority of data for inferring phylogenetic relationships with both concatenation and coalescent methods. However, DNA sequences are susceptible to extensive homoplasy, especially for deep divergences in the Tree of Life. Retroelement insertions have emerged as a powerful alternative to sequences for deciphering evolutionary relationships because these data are nearly homoplasy-free. In addition, retroelement insertions satisfy the “no intralocus-recombination” assumption of summary coalescent methods because they are singular events and better approximate neutrality relative to DNA loci commonly sampled in phylogenomic studies. Retroelements have traditionally been analyzed with parsimony, distance, and network methods. Here, we analyze retroelement data sets for vertebrate clades (Placentalia, Laurasiatheria, Balaenopteroidea, Palaeognathae) with 2 ILS-aware methods that operate by extracting, weighting, and then assembling unrooted quartets into a species tree. The first approach constructs a species tree from retroelement bipartitions with ASTRAL, and the second method is based on split-decomposition with parsimony. We also develop a Quartet-Asymmetry test to detect hybridization using retroelements. Both ILS-aware methods recovered the same species-tree topology for each data set. The ASTRAL species trees for Laurasiatheria have consecutive short branch lengths in the anomaly zone whereas Palaeognathae is outside of this zone. For the Balaenopteroidea data set, which includes rorquals (Balaenopteridae) and gray whale (Eschrichtiidae), both ILS-aware methods resolved balaeonopterids as paraphyletic. Application of the Quartet-Asymmetry test to this data set detected 19 different quartets of species for which historical introgression may be inferred. Evidence for introgression was not detected in the other data sets. 

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2. Structurally Diverse Sampling for Sample-Efficient Training and Comprehensive Evaluation

   https://doi.org/10.18653/v1/2022.findings-emnlp.365  

   Gupta, Shivanshu; Singh, Sameer; Gardner, Matt (January 2022, Findings of the Association for Computational Linguistics: EMNLP)

   A growing body of research has demonstrated the inability of NLP models to generalize compositionally and has tried to alleviate it through specialized architectures, training schemes, and data augmentation, among other approaches. In this work, we study a different approach: training on instances with diverse structures. We propose a model-agnostic algorithm for subsampling such sets of instances from a labeled instance pool with structured outputs. Evaluating on both compositional template splits and traditional IID splits of 5 semantic parsing datasets of varying complexity, we show that structurally diverse training using our algorithm leads to comparable or better generalization than prior algorithms in 9 out of 10 dataset-split type pairs. In general, we find structural diversity to consistently improve sample efficiency compared to random train sets. Moreover, we show that structurally diverse sampling yields comprehensive test sets that are a lot more challenging than IID test sets. Finally, we provide two explanations for improved generalization from diverse train sets: 1) improved coverage of output substructures, and 2) a reduction in spurious correlations between these substructures. 

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3. SPlit: An Optimal Method for Data Splitting

   https://doi.org/10.1080/00401706.2021.1921037  

   Joseph, V. Roshan; Vakayil, Akhil (January 2021, Technometrics)

   null (Ed.)

   In this article, we propose an optimal method referred to as SPlit for splitting a dataset into training and testing sets. SPlit is based on the method of support points (SP), whichwas initially developed for finding the optimal representative points of a continuous distribution. We adapt SP for subsampling from a dataset using a sequential nearest neighbor algorithm. We also extend SP to deal with categorical variables so that SPlit can be applied to both regression and classification problems. The implementation of SPlit on real datasets shows substantial improvement in the worst-case testing performance for several modeling methods compared to the commonly used random splitting procedure. 

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4. Using all Gene Families Vastly Expands Data Available for Phylogenomic Inference

   https://doi.org/10.1093/molbev/msac112  

   Smith, Megan L.; Vanderpool, Dan; Hahn, Matthew W. (June 2022, Molecular Biology and Evolution)

   Townsend, Jeffrey (Ed.)

   Abstract Traditionally, single-copy orthologs have been the gold standard in phylogenomics. Most phylogenomic studies identify putative single-copy orthologs using clustering approaches and retain families with a single sequence per species. This limits the amount of data available by excluding larger families. Recent advances have suggested several ways to include data from larger families. For instance, tree-based decomposition methods facilitate the extraction of orthologs from large families. Additionally, several methods for species tree inference are robust to the inclusion of paralogs and could use all of the data from larger families. Here, we explore the effects of using all families for phylogenetic inference by examining relationships among 26 primate species in detail and by analyzing five additional data sets. We compare single-copy families, orthologs extracted using tree-based decomposition approaches, and all families with all data. We explore several species tree inference methods, finding that identical trees are returned across nearly all subsets of the data and methods for primates. The relationships among Platyrrhini remain contentious; however, the species tree inference method matters more than the subset of data used. Using data from larger gene families drastically increases the number of genes available and leads to consistent estimates of branch lengths, nodal certainty and concordance, and inferences of introgression in primates. For the other data sets, topological inferences are consistent whether single-copy families or orthologs extracted using decomposition approaches are analyzed. Using larger gene families is a promising approach to include more data in phylogenomics without sacrificing accuracy, at least when high-quality genomes are available. 

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5. Multi‐mask self‐supervised learning for physics‐guided neural networks in highly accelerated magnetic resonance imaging

   https://doi.org/10.1002/nbm.4798  

   Yaman, Burhaneddin; Gu, Hongyi; Hosseini, Seyed Amir; Demirel, Omer Burak; Moeller, Steen; Ellermann, Jutta; Uğurbil, Kâmil; Akçakaya, Mehmet (December 2022, NMR in Biomedicine)

   Self‐supervised learning has shown great promise because of its ability to train deep learning (DL) magnetic resonance imaging (MRI) reconstruction methods without fully sampled data. Current self‐supervised learning methods for physics‐guided reconstruction networks split acquired undersampled data into two disjoint sets, where one is used for data consistency (DC) in the unrolled network, while the other is used to define the training loss. In this study, we propose an improved self‐supervised learning strategy that more efficiently uses the acquired data to train a physics‐guided reconstruction network without a database of fully sampled data. The proposed multi‐mask self‐supervised learning via data undersampling (SSDU) applies a holdout masking operation on the acquired measurements to split them into multiple pairs of disjoint sets for each training sample, while using one of these pairs for DC units and the other for defining loss, thereby more efficiently using the undersampled data. Multi‐mask SSDU is applied on fully sampled 3D knee and prospectively undersampled 3D brain MRI datasets, for various acceleration rates and patterns, and compared with the parallel imaging method, CG‐SENSE, and single‐mask SSDU DL‐MRI, as well as supervised DL‐MRI when fully sampled data are available. The results on knee MRI show that the proposed multi‐mask SSDU outperforms SSDU and performs as well as supervised DL‐MRI. A clinical reader study further ranks the multi‐mask SSDU higher than supervised DL‐MRI in terms of signal‐to‐noise ratio and aliasing artifacts. Results on brain MRI show that multi‐mask SSDU achieves better reconstruction quality compared with SSDU. The reader study demonstrates that multi‐mask SSDU at R = 8 significantly improves reconstruction compared with single‐mask SSDU at R = 8, as well as CG‐SENSE at R = 2. 

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