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  1. ...Single-nucleus multiomic profiling of the aging mouse substantia nigra reveals conserved gene alterations linked to Parkinson’s disease Kangli Wang,1 Weikun Xia,1 Yingli Gu,1 Songpeng Zu,1 Qian Yang,2 Maria Luisa Amaral,1 Yaozhi Wang,1 Allen Wang,2 Xiang-Dong Fu,3 William C. Mobley,4 and Bing Ren1...
  2. ...are usually lost over short evolutionary timescales, but they can be retained through three primary mechanisms: conservation of wild-type function, in which duplicates alter gene dosage or provide redundancy; subfunctionalization, in which ancestral function is partitioned across copies...
  3. ...transposition. Following post-GEM cleanup, libraries were preamplified by PCR, after which the sample was split into three parts: one part generated the snRNA-seq library, one part generated the snATAC-seq library, and the rest was kept at −20°C. SnATAC and snRNA libraries were indexed for multiplexing...
  4. ...and then quantified by quantitative polymerase chain reaction (PCR). Hi-C sequencing was performed by a Illumina HiSeq 2500 platform, using the paired-end of 150 bp reads.To assist gene prediction and dosage compensation analysis, 24 RNA-seq libraries were generated from brain, hindleg, and gonads with four...
  5. ...RNAs (Supplemental Fig. S12), underlining the crucial role of motif conservation in snoRNP formation. Overall, these results suggest that box sequence conservation (especially the C, H, and ACA motifs), snoRNA stability (global structure and at the terminal stem level), and host gene expression level...
  6. ...in genetic diversity and gene regulation, and are associated with various neurological and developmental disorders. They can also arise in sequencing reads generated by certain technologies, such as those used for sequencing circular molecules. A key challenge in analyzing tandem repeats is reconstructing...
  7. ...al. 2021b) and have biological significance. Additionally, primes could serve practical purposes, such as PCR primers, highly specific platforms in CRISPR construct designs, genomic barcodes, and sample labeling. Previous studies examined a limited number of s and derived 60,370 15 bp nucleic prime...
  8. ...using the NEB Ultra II directional RNA library prep kit with sample purification beads (NEB E7765), with 10–14 PCR cycles (determined empirically to achieve the minimum number of cycles per library). Libraries were then sequenced on an Illumina HiSeq 2000 in single-end mode, except for the 12 h time...
  9. ...processed as for CNV (trimmed for adapter sequences, aligned with Burrows-Wheeler Aligner 0.7.18, and PCR duplicates removed). Mapped, filtered, and deduplicated reads were counted into genomic windows of distinct size (from 5- to 100-kb) using the intersect function from BEDTools 2.31.1 (Quinlan and Hall...
  10. ...analysis reveals candidate TFs acting via endoderm HCNE CRMs. (A,B) High-confidence de novo motifs enriched in HCNEs overlapping both human PFG H3K27ac peaks and sox17E > sox17M DARs at 28 and/or 48 hpf for the human (A) and zebrafish (B) HCNE sequences. Pvalues and closest match vertebrate TFs assigned...
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