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Kamil Antoszewski, Klaudia Chmielewska, Karolina Jagiełło, Tomasz Puzyn
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CRISPR–Cas9: a history of its discovery and ethical considerations of its use in genome Editing
2022
10.1038/nrd.2017.243
10.1038/nrd.2017.243
10.1038/s41587-022-01294-2
10.1038/s41587-022-01294-2
A deep learning framework for exploring similar patterns in DNA N6-methyladenine sites across different species
2021
10.1038/s41586-021-03819-2
10.1038/s41586-021-03819-2
Ligandability and druggability assessment via machine learning
10.1002/wcms.1676 · 2023
Machine learning approaches for predicting protein-ligand binding sites from sequence data
10.3389/fbinf.2025.1520382 · 2025
To metabolomics and beyond: a technological portfolio to investigate cancer metabolism
2023
10.1038/s41374-022-00830-7
10.1038/s41374-022-00830-7
High-Throughput Metabolomics for Identification of Metabolic Pathways and Deciphering the Effect Mechanism of Dioscin on Rectal Cancer From Cell Metabolic Profiles Coupled With Chemometrics Analysis
2020
Confidence 95%
unpaywall
Confidence 95%
doaj
Confidence 92%
datacite
Confidence 0%
10.1038/s41385-022-00553-4
10.1038/s41385-022-00553-4
Hill Catherine Prediction of cancer outcome with microarrays: a multiple random validation strategy
10.1016/s0140-6736(05)17866-0 · 2005
More is better: Recent progress in multi-omics data integration methods
10.3389/fgene.2017.00084 · 2017
10.1007/s00204-021-03031-1
10.1007/s00204-021-03031-1
10.1038/s41576-019-0150-2
10.1038/s41576-019-0150-2
Snyder Michael RNA-Seq: a revolutionary tool for transcriptomics
10.1038/nrg2484 · 2009
10.1038/nbt.1621
10.1038/nbt.1621
A survey of best practices for RNA-seq data analysis
2016
Opportunities and challenges in long-read sequencing data analysis
10.1186/s13059-020-1935-5 · 2020
Highly parallel direct RN A sequencing on an array of nanopores
10.1038/nmeth.4577 · 2018
A practical guide to single-cell RNA-sequencing for biomedical research and clinical applications
10.1186/s13073-017-0467-4 · 2017
Unresolved referenced work
Kept as external metadata until matched
Predictive biomarkers for embryotoxicity: a machine learning approach to mitigating multicollinearity in RNA-Seq
10.1007/s00204-024-03852-w · 2024
Evaluating the performance of multi-omics integration: a thyroid toxicity case study
10.1007/s00204-024-03876-2 · 2025
10.1007/s00204-020-02656-y
10.1007/s00204-020-02656-y
10.1111/mec.15797
10.1111/mec.15797
Whole genome re-sequencing in 437 tobacco germplasms identifies plant height candidate genes
2025
RNA sequencing reveals transcriptomic changes in tobacco (Nicotiana tabacum) following NtCPS2 knockdown
2021
RNA-seq data science: From raw data to effective interpretation
10.3389/fgene.2023.997383 · 2023
RNA-seq and microarray complement each other in transcriptome profiling
10.1186/1471-2164-13-629 · 2012
10.1016/j.cmet.2016.08.018
10.1016/j.cmet.2016.08.018
mRNA-seq whole transcriptome profiling of fresh frozen versus archived fixed tissues
2018
Ultra-affordable high-throughput transcriptomics enabled by bulk RNA barcoding and sequencing
10.1186/s13059-019-1671-x · 2019
10.1016/j.cell.2015.05.002
10.1016/j.cell.2015.05.002
10.1038/nmeth.1315
10.1038/nmeth.1315
10.1038/nbt.2859
10.1038/nbt.2859
Single-cell RNA sequencing technologies and applications: A brief overview
10.1002/ctm2.694 · 2022
10.1038/nmeth.4220
10.1038/nmeth.4220
10.1126/science.aaf2403
10.1126/science.aaf2403
10.1038/s41592-020-01033-y
10.1038/s41592-020-01033-y
recount3: summaries and queries for large-scale RNA-seq expression and splicing
10.1186/s13059-021-02533-6 · doi-reference
The sequence read archive: Explosive growth of sequencing data
10.1093/nar/gkr854 · doi-reference
10.1093/nar/gkab1053
10.1093/nar/gkab1053 · doi-reference
Expression Atlas update: Gene and protein expression in multiple species
10.1093/nar/gkab1030 · doi-reference
From ArrayExpress to BioStudies
10.1093/nar/gkaa1062 · doi-reference
10.1093/nar/gky964
10.1093/nar/gky964 · doi-reference
10.1093/nar/gkx965
10.1093/nar/gkx965 · doi-reference
The BioStudies database
10.15252/msb.20156658 · doi-reference
10.1093/nar/gkad965
10.1093/nar/gkad965 · doi-reference
10.1093/nar/30.1.207
10.1093/nar/30.1.207 · doi-reference
Detecting and correcting systematic variation in large-scale RNA sequencing data
10.1038/nbt.3000 · doi-reference
Integrative genomics viewer
10.1038/nbt.1754 · doi-reference
10.1093/bioinformatics/btt656
10.1093/bioinformatics/btt656 · doi-reference
10.1101/2025.05.21.655404
10.1101/2025.05.21.655404 · doi-reference
10.1038/nbt.3122
10.1038/nbt.3122 · doi-reference
10.1038/nbt.1883
10.1038/nbt.1883 · doi-reference
10.1093/bioinformatics/bts094
10.1093/bioinformatics/bts094 · doi-reference
10.1093/bioinformatics/btu077
10.1093/bioinformatics/btu077 · doi-reference
10.1093/bioinformatics/bti610
10.1093/bioinformatics/bti610 · doi-reference
10.1093/bioinformatics/btq057
10.1093/bioinformatics/btq057 · doi-reference
SOAPsplice: Genome-wide ab initio detection of splice junctions from RNA-Seq data
10.3389/fgene.2011.00046 · doi-reference
10.1038/nprot.2013.084
10.1038/nprot.2013.084 · doi-reference
10.1093/bioinformatics/bty191
10.1093/bioinformatics/bty191 · doi-reference
10.1093/bioinformatics/btp324
10.1093/bioinformatics/btp324 · doi-reference
Impact of gene annotation choice on the quantification of RNA-seq data
10.1186/s12859-022-04644-8 · doi-reference
10.1038/s41587-019-0201-4
10.1038/s41587-019-0201-4 · doi-reference
Genome tools: A comprehensive software library for efficient processing of structured genome annotations
10.1109/tcbb.2013.68 · doi-reference
10.1093/bioinformatics/btw354
10.1093/bioinformatics/btw354 · doi-reference
10.1093/bioinformatics/bts635
10.1093/bioinformatics/bts635 · doi-reference
10.1093/bioinformatics/btr026
10.1093/bioinformatics/btr026 · doi-reference
Flexbar 3.0 - SIMD and multicore parallelization
10.1093/bioinformatics/btx330 · doi-reference
Ultrafast one-pass FASTQ data preprocessing, quality control, and deduplication using fastp
10.1002/imt2.107 · doi-reference
A Quick Introduction to Version Control with Git and GitHub
10.1371/journal.pcbi.1004668 · doi-reference
International cancer genome consortium data portal-a one-stop shop for cancer genomics data
10.1093/database/bar026 · doi-reference
variancePartition: Interpreting drivers of variation in complex gene expression studies
10.1186/s12859-016-1323-z · doi-reference
10.1186/s13059-014-0550-8
10.1186/s13059-014-0550-8 · doi-reference
10.1093/nar/gkv007
10.1093/nar/gkv007 · doi-reference
10.1093/biostatistics/kxj037
10.1093/biostatistics/kxj037 · doi-reference
10.1038/nbt.2931
10.1038/nbt.2931 · doi-reference
Batch effect detection and correction in RNA-seq data using machine-learning-based automated assessment of quality
10.1186/s12859-022-04775-y · doi-reference