Study highlights strategies for faster detection of SARS-CoV-2 variants.
― 6 min read
Cutting edge science explained simply
Study highlights strategies for faster detection of SARS-CoV-2 variants.
― 6 min read
Research reveals new tools for studying RNA virus genetic exchanges.
― 5 min read
doubletrouble offers a user-friendly approach to studying gene duplications and their implications in evolution.
― 5 min read
A novel tool to simplify nanopore sequencing data interpretation.
― 7 min read
GeneGPT enhances language models for accurate genomic answers using NCBI APIs.
― 5 min read
New algorithm improves understanding of complex satellite DNA structures.
― 6 min read
Researchers assess DNA variant calling tools using synthetic data for cancer studies.
― 6 min read
New tools improve accuracy in bacterial genome assembly.
― 5 min read
hAMRonization aims to improve AMR detection accuracy through standardized data.
― 5 min read
RNA3DB aims to improve RNA structure prediction using a new organized dataset.
― 5 min read
Introducing LIN codes to improve bacterial strain classification and tracking.
― 6 min read
Research uncovers patterns of chromosomal changes linked to various cancer types.
― 8 min read
Genomic data enhances tracking and understanding of disease spread and dynamics.
― 6 min read
Examining how software tools improve viral genome assembly using next-generation sequencing.
― 6 min read
A new method improves insights into gene interactions and spatial dependencies in tissues.
― 5 min read
BOSS offers faster, reliable solutions for finding optimal biomarker cutoffs.
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Research reveals key insights into the SAR86 bacteria's characteristics and ecological role.
― 5 min read
CARAMEL offers efficient storage and fast access for large data sets.
― 5 min read
BayeLeafClassifier offers precise cell identification in single-cell RNA sequencing.
― 6 min read
A novel approach improves insights into gene activity in individual cells.
― 7 min read
A study comparing genome assembly methods for various nematode species.
― 6 min read
scEmbed streamlines single-cell chromatin accessibility analysis using pre-trained models.
― 6 min read
New methods improve gene interaction analysis from single-cell RNA sequencing data.
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An overview of the methods used to reconstruct sequences from substrings.
― 5 min read
Researchers work to combat species loss using genomic techniques.
― 7 min read
New methods aim to improve data consistency and collaboration in cell atlas projects.
― 6 min read
Chronumental allows quick analysis of large virus datasets through time trees.
― 5 min read
Using autoencoders to enhance accuracy in SNP variant detection.
― 6 min read
hictk simplifies working with Hi-C and Cooler file formats for researchers.
― 5 min read
New method improves accuracy of sequence alignments in fragmented genomic data.
― 6 min read
A new method simplifies SNP identification in pathogen genomes.
― 7 min read
New methods enhance the speed of genomic data analysis using SBWT and LCP array.
― 4 min read
A comprehensive dataset aids research on cancer cells and immune checkpoint therapy.
― 6 min read
Exploring methods to extract signals from noisy datasets across various fields.
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BuDDI improves insights from RNA sequencing data by combining bulk and single-cell analysis.
― 6 min read
A new method improves genome assembly using both long and short DNA reads.
― 4 min read
New models predict protein functions and mutations to improve health responses.
― 8 min read
Unico improves analysis of complex genomic data with a flexible approach.
― 6 min read
New tools enhance understanding of complex biological data.
― 6 min read
K-mer methods play a key role in genomic studies and data analysis.
― 6 min read