ViMIC: a database of human disease-related virus mutations, integration sites and cis-effects.
PMID:34500462
Where are G-quadruplexes located in the human transcriptome?
PMID:33575590
Comprehensive Profiling of Gene Expression in the Cerebral Cortex and Striatum of BTBRTF/ArtRbrc Mice Compared to C57BL/6J Mice.
PMID:33362469
Transcriptomics in Toxicogenomics, Part II: Preprocessing and Differential Expression Analysis for High Quality Data.
PMID:32397130
A systematic evaluation of single cell RNA-seq analysis pipelines.
PMID:31604912
Beyond sequencing: re-visiting annotations for PJL as a test case.
PMID:31366397
Genetic, Inflammatory, and Epithelial Cell Differentiation Factors Control Expression of Human Calpain-14.
PMID:30626591
Two novel colorectal cancer risk loci in the region on chromosome 9q22.32.
PMID:29541405
TERIUS: accurate prediction of lncRNA via high-throughput sequencing data representing RNA-binding protein association.
PMID:29504902
Inferring the evolution of the major histocompatibility complex of wild pigs and peccaries using hybridisation DNA capture-based sequencing.
PMID:29256177
scRNASeqDB: A Database for RNA-Seq Based Gene Expression Profiles in Human Single Cells.
PMID:29206167
A Computational Methodology to Overcome the Challenges Associated With the Search for Specific Enzyme Targets to Develop Drugs Against Leishmania major.
PMID:28638238
De novo RNA sequence assembly during in vivo inflammatory stress reveals hundreds of unannotated lincRNAs in human blood CD14+ monocytes and in adipose tissue.
PMID:28389524
Genomic structure of the horse major histocompatibility complex class II region resolved using PacBio long-read sequencing technology.
PMID:28361880
Identification of long non-coding transcripts with feature selection: a comparative study.
PMID:28335739
A fuzzy method for RNA-Seq differential expression analysis in presence of multireads.
PMID:28185579
The state of play in higher eukaryote gene annotation.
PMID:27773922
The Effect of Human Genome Annotation Complexity on RNA-Seq Gene Expression Quantification.
PMID:27532059
Thousands of novel translated open reading frames in humans inferred by ribosome footprint profiling.
PMID:27232982
Topology based identification and comprehensive classification of four-transmembrane helix containing proteins (4TMs) in the human genome.
PMID:27030248
Genome-Wide Identification and Characterization of Long Non-Coding RNAs from Mulberry (Morus notabilis) RNA-seq Data.
PMID:26938562
In Silico Functional Annotation of Genomic Variation.
PMID:26724722
Ensembl 2016.
PMID:26687719
DANIO-CODE: Toward an Encyclopedia of DNA Elements in Zebrafish.
PMID:26671609
Towards improved genome-scale metabolic network reconstructions: unification, transcript specificity and beyond.
PMID:26615025
Comprehensive comparative homeobox gene annotation in human and mouse.
PMID:26412852
Orthology for comparative genomics in the mouse genome database.
PMID:26223881
Mouse Genome Database: From sequence to phenotypes and disease models.
PMID:26150326
Informatics resources for the Collaborative Cross and related mouse populations.
PMID:26135136
A unified gene catalog for the laboratory mouse reference genome.
PMID:26084703
BCR repertoire sequencing: different patterns of B-cell activation after two Meningococcal vaccines.
PMID:25976772
A comprehensive evaluation of ensembl, RefSeq, and UCSC annotations in the context of RNA-seq read mapping and gene quantification.
PMID:25765860
Immunoglobulins: 25 years of immunoinformatics and IMGT-ONTOLOGY.
PMID:25521638
Identification of antigen-specific B cell receptor sequences using public repertoire analysis.
PMID:25392534
Discovery Genetics - The History and Future of Spontaneous Mutation Research.
PMID:25364627
Renal Gene Expression Database (RGED): a relational database of gene expression profiles in kidney disease.
PMID:25252782
Hypoxia adaptations in the grey wolf (Canis lupus chanco) from Qinghai-Tibet Plateau.
PMID:25078401
GeneSense: a new approach for human gene annotation integrated with protein-protein interaction networks.
PMID:24667292
Immunoglobulin and T Cell Receptor Genes: IMGT(®) and the Birth and Rise of Immunoinformatics.
PMID:24600447
Assessing the impact of human genome annotation choice on RNA-seq expression estimates.
PMID:24564364
Ensembl 2014.
PMID:24316576
The Vertebrate Genome Annotation browser 10 years on.
PMID:24316575
ExoLocator--an online view into genetic makeup of vertebrate proteins.
PMID:24271393
Alzheimer's disease: analyzing the missing heritability.
PMID:24244562
Current status and new features of the Consensus Coding Sequence database.
PMID:24217909
Functional transcriptomics in the post-ENCODE era.
PMID:24172201
The mouse Gene Expression Database (GXD): 2014 update.
PMID:24163257
The tiger genome and comparative analysis with lion and snow leopard genomes.
PMID:24045858
The relationship between gene isoform multiplicity, number of exons and protein divergence.
PMID:24023641
Comprehensive characterization of 10,571 mouse large intergenic noncoding RNAs from whole transcriptome sequencing.
PMID:23951020
Fine mapping of type 1 diabetes regions Idd9.1 and Idd9.2 reveals genetic complexity.
PMID:23934554
Detecting and comparing non-coding RNAs in the high-throughput era.
PMID:23887659
Gene fusion analysis in the battle against the African endemic sleeping sickness.
PMID:23874788
Transcriptome analyses of the human retina identify unprecedented transcript diversity and 3.5 Mb of novel transcribed sequence via significant alternative splicing and novel genes.
PMID:23865674
Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy.
PMID:23806086
An automated algorithm for extracting functional immunologic V-genes from genomes in jawed vertebrates.
PMID:23793106
The non-obese diabetic mouse sequence, annotation and variation resource: an aid for investigating type 1 diabetes.
PMID:23729657
Sequencing and comparative analysis of the gorilla MHC genomic sequence.
PMID:23589541
iSeeRNA: identification of long intergenic non-coding RNA transcripts from transcriptome sequencing data.
PMID:23445546
The genomic signature of trait-associated variants.
PMID:23418889
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors.
PMID:23407934
Finding protein-coding genes through human polymorphisms.
PMID:23349826
Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing.
PMID:23255406
Gene family matters: expanding the HGNC resource.
PMID:23245209
Long-range transcriptome sequencing reveals cancer cell growth regulatory chimeric mRNA.
PMID:23226102
Ensembl 2013.
PMID:23203987
GenomeRNAi: a database for cell-based and in vivo RNAi phenotypes, 2013 update.
PMID:23193271
PeroxiBase: a database for large-scale evolutionary analysis of peroxidases.
PMID:23180785
Genenames.org: the HGNC resources in 2013.
PMID:23161694
Prediction of altered 3'- UTR miRNA-binding sites from RNA-Seq data: the swine leukocyte antigen complex (SLA) as a model region.
PMID:23139801
The IMGT/HLA database.
PMID:23080122
AbsIDconvert: an absolute approach for converting genetic identifiers at different granularities.
PMID:22967011
GENCODE: the reference human genome annotation for The ENCODE Project.
PMID:22955987
Combining RT-PCR-seq and RNA-seq to catalog all genic elements encoded in the human genome.
PMID:22955982
29 mammalian genomes reveal novel exaptations of mobile elements for likely regulatory functions in the human genome.
PMID:22952639
The GENCODE pseudogene resource.
PMID:22951037
MiR-25 regulates Wwp2 and Fbxw7 and promotes reprogramming of mouse fibroblast cells to iPSCs.
PMID:22912667
Incorporating RNA-seq data into the zebrafish Ensembl genebuild.
PMID:22798491
The yak genome and adaptation to life at high altitude.
PMID:22751099
The male germ cell gene regulator CTCFL is functionally different from CTCF and binds CTCF-like consensus sites in a nucleosome composition-dependent manner.
PMID:22709888
IMGT-ONTOLOGY 2012.
PMID:22654892
O-miner: an integrative platform for automated analysis and mining of -omics data.
PMID:22600742
SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update).
PMID:22544707
The importance of identifying alternative splicing in vertebrate genome annotation.
PMID:22434846
Community gene annotation in practice.
PMID:22434843
Tracking and coordinating an international curation effort for the CCDS Project.
PMID:22434842
Evidence for transcript networks composed of chimeric RNAs in human cells.
PMID:22238572
Isolation of homozygous mutant mouse embryonic stem cells using a dual selection system.
PMID:22127858
Ensembl 2012.
PMID:22086963
The UCSC Genome Browser.
PMID:21975940
RNAcentral: A vision for an international database of RNA sequences.
PMID:21940779
Consequences of the discontinuation of the International Protein Index (IPI) database and its substitution by the UniProtKB "complete proteome" sets.
PMID:21932440
BioMart Central Portal: an open database network for the biological community.
PMID:21930507
Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.
PMID:21787409
Ensembl BioMarts: a hub for data retrieval across taxonomic space.
PMID:21785142
Published and perished? The influence of the searched protein database on the long-term storage of proteomics data.
PMID:21700957
Characterization and improvement of RNA-Seq precision in quantitative transcript expression profiling.
PMID:21685096
A conditional knockout resource for the genome-wide study of mouse gene function.
PMID:21677750
Zebrafish mRNA sequencing deciphers novelties in transcriptome dynamics during maternal to zygotic transition.
PMID:21555364
The origins, evolution, and functional potential of alternative splicing in vertebrates.
PMID:21551269
Saturation of the human phenome.
PMID:21532833
MAISTAS: a tool for automatic structural evaluation of alternative splicing products.
PMID:21498402
Shotgun proteomics aids discovery of novel protein-coding genes, alternative splicing, and "resurrected" pseudogenes in the mouse genome.
PMID:21460061
UniProt Knowledgebase: a hub of integrated protein data.
PMID:21447597
Disease and phenotype data at Ensembl.
PMID:21400687
Transcript catalogs of human chromosome 21 and orthologous chimpanzee and mouse regions.
PMID:21400203
The GENCODE exome: sequencing the complete human exome.
PMID:21364695
Naming 'junk': human non-protein coding RNA (ncRNA) gene nomenclature.
PMID:21296742
The Genomic HyperBrowser: inferential genomics at the sequence level.
PMID:21182759
The mouse Gene Expression Database (GXD): 2011 update.
PMID:21062809
The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics.
PMID:21051359
ZFIN: enhancements and updates to the Zebrafish Model Organism Database.
PMID:21036866
PathEx: a novel multi factors based datasets selector web tool.
PMID:20969778
Genome-wide data-mining of candidate human splice translational efficiency polymorphisms (STEPs) and an online database.
PMID:20948966
The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium.
PMID:20929875
genenames.org: the HGNC resources in 2011.
PMID:20929869
Exploring zebrafish genomic, functional and phenotypic data using ZFIN.
PMID:20836073
Quantifying the mechanisms of domain gain in animal proteins.
PMID:20633280
Integrating heterogeneous sequence information for transcriptome-wide microarray design; a Zebrafish example.
PMID:20626891
Reconstruction and validation of RefRec: a global model for the yeast molecular interaction network.
PMID:20498836
AphidBase: a centralized bioinformatic resource for annotation of the pea aphid genome.
PMID:20482635
Consistent annotation of gene expression arrays.
PMID:20459806
From IMGT-ONTOLOGY to IMGT/LIGMotif: the IMGT standardized approach for immunoglobulin and T cell receptor gene identification and description in large genomic sequences.
PMID:20433708
Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.
PMID:20011118
DASMiner: discovering and integrating data from DAS sources.
PMID:19919683
Ensembl's 10th year.
PMID:19906699
A unique, consistent identifier for alternatively spliced transcript variants.
PMID:19865484
EMAGE mouse embryo spatial gene expression database: 2010 update.
PMID:19767607
The completion of the Mammalian Gene Collection (MGC).
PMID:19767417
The cadherin superfamily and epileptogenesis: end of the beginning?
PMID:19471581
Sim4cc: a cross-species spliced alignment program.
PMID:19429899
Cross-species mapping of bidirectional promoters enables prediction of unannotated 5' UTRs and identification of species-specific transcripts.
PMID:19393065
Identifying protein-coding genes in genomic sequences.
PMID:19226436
Annotation of mammalian primary microRNAs.
PMID:19038026
Ensembl 2009.
PMID:19033362
Genome and proteome annotation: organization, interpretation and integration.
PMID:19019817
INTERFEROME: the database of interferon regulated genes.
PMID:18996892
G2Cdb: the Genes to Cognition database.
PMID:18984621
IMGT, the international ImMunoGeneTics information system.
PMID:18978023
PEDANT covers all complete RefSeq genomes.
PMID:18940859
Splice-mediated Variants of Proteins (SpliVaP) - data and characterization of changes in signatures among protein isoforms due to alternative splicing.
PMID:18831736