Searching journal content for articles similar to Hildmann et al. 9 (4): 360.

Displaying results 1-10 of 6149
For checked items
  1. ...lymphoma (DLBCL) data set in which we integrate SWATH-MS-based proteomics with transcriptomic and phenotypic data.State-of-the-art proteomic approaches such as liquid chromatography coupled to quadrupole-time of flight tandem mass spectrometry (LC-QTOF-MS/MS) facilitate the high-throughput characterization...
  2. ...-read sequencing allows for high-throughput characterization of the locus, and efforts are underway to gather germline diversity across human populations (Rodriguez et al. 2020). However, although this strategy yields highly accurate reads, it does not contiguously resolve the entirety of the locus and may miss...
  3. ...has adapted to thrive in animal hosts with different diets, physiologies, and resident microbiota. Our highly contiguous and complete s allowed us to investigate patterns of evolution within and between subtypes and to compare the genus to related protists. This work demonstrates how high...
  4. ...and ancestry inference. Utilizing feature selection and machine learning methods, HITSNP effectively and reliably screens feature SNPs representing breed diversity from high-throughput data. Furthermore, we have outlined a pipeline for predicting the number and composition of ancestors based on a reference...
  5. ...enhancers in the brain, which identified ∼79,000 brain-specific enhancers (Wang et al. 2018). We identified a high-confidence set of PFC enhancers (18,212 regions) based on strong ATAC-seq and DNase signals, as well as strong H3K27ac signals from both the Roadmap PFC and PsychENCODE PFC ChIP-seq experiments...
  6. ...of noncoding genetic variants and the decoding of regulatory element architecture (Zhou and Troyanskaya 2015; Kelley et al. 2018; Avsec et al. 2021a; Pampari et al. 2024). Accurate, high-resolution maps of chromatin accessibility are essential for downstream tasks such as identifying regulatory elements...
  7. ...transgenesis, site-specific recombinases, ZFN, TALEN, and CRISPR-Cas9, as well as a high-throughput CRISPR library screening platform in cultured B. mori cells (Ma et al. 2012, 2013, 2014b; Duan et al. 2013; Liu et al. 2014, 2018; Chang et al. 2020a). However, because the accumulation of genetic resources...
  8. ...CRISPR-Cas9-based repeat depletion for high-throughput genotyping of complex plant s Marzia Rossato1,2,6, Luca Marcolungo1,6, Luca De Antoni1, Giulia Lopatriello1, Elisa Bellucci3, Gaia Cortinovis3, Giulia Frascarelli3, Laura Nanni3, Elena Bitocchi3, Valerio Di Vittori3, Leonardo Vincenzi1, Filippo...
  9. ...). Interestingly, 90% of the high-confident 5′-DRACH-3′ sites detected in the present study are also deposited in RMBase v.3.0 and therefore represent modifications validated by antibody-based high-throughput sequencing methodologies (Fig. 1F). Motif analysis of the obtained nanopore sequencing data revealed...
  10. ...-truth sequences. It compares favorably to the existing methods. MethodsOverviewOur method, pan-based haplotype inference (PHI), takes as input a pan graph reference and short-read sequencing data from a target haploid . We assume that the given pan graph has been constructed using high-quality, haplotype...
For checked items

Preprint Server