bioRxiv Science⌕ Search

Biology subjects

Regnier, A.

Publications and source records attributed to Regnier, A..

3 recordsLinked to original sources

Lossless compression of k-mer matrices enabling random row access

Genomic search engines such as Logan-Search index petabytes of sequencing data as large binary matrices, called k-mer matrices, where each row encodes the presence of a k-mer across thousands to millions of genomic samples. Logan-Search contains a petabyte of binary matrices, and storing them is expensive, yet compression must not prevent fast random access to any matrix row at query time. We present kmcomp, a lossless compression method for k-mer matrices that satisfies these competing requirements. Block compression partitions the matrix into fixed-size row blocks, each compressed independently; block start positions are stored in an Elias-Fano encoded array, enabling O(1) random access to any block. To improve compressibility without introducing additional decompression steps, we introduce the{pi} -compression: a column reordering that groups similar samples together by solving the Traveling Salesman Problem via a nearest-neighbor heuristic. We accelerate this heuristic with a novel variant of the vantage-point tree, the masked vp-tree, which dynamically prunes nearest-neighbor search space. On three (meta)genomic datasets, kmcomp achieves compression ratios of 1.3 to 5.4;{pi} -compression further improves these to 1.5 to 51.3. Applied to the Logan-Search petabyte-scale index, compression reduces storage by approximately half, and{pi} -compression adds a further 13% gain. Query overhead remains modest: queries of hundreds of nucleotides incur an absolute latency increase of{approx} 100 ms, and highly compressed indexes can match uncompressed query times thanks to reduced disk reads.

bioinformatics↗

YAP-dependent autophagy is controlled by AMPK, SIRT1 and flow intensity in kidney epithelial cells.

Shear stress generated by the urinary fluid flow is an important regulator of renal function. Its dysregulation is observed in various chronic and acute kidney diseases. Previously, we demonstrated that primary cilium-dependent autophagy allows kidney epithelial cells to adapt their metabolism in response to fluid flow. Here, we show that nuclear YAP/TAZ negatively regulates autophagy machinery in kidney epithelial cells subjected to fluid flow. This crosstalk is supported by a primary cilium-dependent activation of AMPK and SIRT1, independently of the Hippo pathway. We confirmed the relevance of the YAP/TAZ-autophagy molecular dialog in vivo using a zebrafish model of kidney development and a unilateral ureteral obstruction mouse model. In addition, an in vitro assay simulating the pathological flow observed at early stages of chronic kidney disease (CKD) activated YAP, leading to a primary cilium-dependent inhibition of autophagy. Our findings demonstrate the importance of YAP/TAZ and autophagy in the translation of fluid flow into cellular and physiological responses. Dysregulation of this pathway is associated with the early onset of CKD.

cell biology↗

Children cooperate more successfully with non-kin than with siblings.

Cooperation plays a key role in advanced societies with human cooperation among kin being more prominent than cooperation among non-kin. However, little is known about the developmental roots of kin and non-kin cooperation in humans. Here, we show for the first time that children cooperated less successfully with siblings than with non-kin children, whether or not non-kin partners were friends. Furthermore, children with larger social networks cooperated better and the perception of friendship among non-friends improved after cooperating. These results indicate that non-kin cooperation in humans has deep developmental foundations which might serve to forge and extend non-kin social relationships during middle childhood and create opportunities for future collaboration beyond kin. Our results provide a new framework for future studies focusing on how and why cooperation with different classes of partners may change during development in humans as well as other long-lived organisms.

evolutionary biology↗