| P50 | author | Radka Platte | Q98148377 |
| P2093 | author name string | Joanna Bottomley | |
| | Daniel Barrett | |
| | Diane Gleeson | |
| | Edward Ryder | |
| | James Bussell | |
| | Shaheen Akhtar | |
| | Debarati Sethi | |
| | Michaela Bruntraeger | |
| | Jonathan Burvill | |
| P2860 | cites work | Structure and evolution of the mouse pregnancy-specific glycoprotein (Psg) gene locus | Q21266603 |
| | Robust and sensitive analysis of mouse knockout phenotypes | Q21559650 |
| | A conditional knockout resource for the genome-wide study of mouse gene function | Q21735918 |
| | Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes | Q24597048 |
| | Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project | Q24631734 |
| | Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 |
| | INFRAFRONTIER: a European resource for studying the functional basis of human disease | Q26748700 |
| | Fast gapped-read alignment with Bowtie 2 | Q27860699 |
| | High-throughput engineering of the mouse genome coupled with high-resolution expression analysis | Q28202486 |
| | Improving bioscience research reporting: the ARRIVE guidelines for reporting animal research | Q29547313 |
| | One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering | Q29547524 |
| | Improved protocols for the illumina genome analyzer sequencing system | Q30446288 |
| | Prevalence of sexual dimorphism in mammalian phenotypic traits | Q33851019 |
| | CRISPR/Cas9-mediated gene knockout in the mouse brain using in utero electroporation | Q34046124 |
| | Somatic mosaicism and allele complexity induced by CRISPR/Cas9 RNA injections in mouse zygotes | Q34200242 |
| | High resolution melt analysis (HRMA); a viable alternative to agarose gel electrophoresis for mouse genotyping | Q34428490 |
| | Reproducibility: use mouse biobanks or lose them | Q35660335 |
| | Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders | Q35793513 |
| | Efficient identification of CRISPR/Cas9-induced insertions/deletions by direct germline screening in zebrafish | Q35968268 |
| | Analysis of the mouse gut microbiome using full-length 16S rRNA amplicon sequencing | Q36076542 |
| | Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction | Q36096483 |
| | Failure to Genotype: A Cautionary Note on an Elusive loxP Sequence | Q36170789 |
| | High-throughput genotyping of CRISPR/Cas9-mediated mutants using fluorescent PCR-capillary gel electrophoresis | Q36205889 |
| | High-throughput sequencing of multiple amplicons for barcoding and integrative taxonomy | Q36271269 |
| | Next-generation sequencing of experimental mouse strains | Q36296093 |
| | Chromosome engineering in zygotes with CRISPR/Cas9. | Q36762223 |
| | Molecular characterization of mutant mouse strains generated from the EUCOMM/KOMP-CSD ES cell resource | Q37100323 |
| | Rapid conversion of EUCOMM/KOMP-CSD alleles in mouse embryos using a cell-permeable Cre recombinase | Q37471738 |
| | High-throughput discovery of novel developmental phenotypes | Q37629635 |
| | Efficient and rapid generation of large genomic variants in rats and mice using CRISMERE | Q37683801 |
| | Pregnancy-specific glycoproteins: complex gene families regulating maternal-fetal interactions | Q38229473 |
| | Genome-wide in vivo screen identifies novel host regulators of metastatic colonization | Q38723015 |
| | Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control | Q39212049 |
| | A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. | Q42375961 |
| | Using the mouse to model human disease: increasing validity and reproducibility | Q42599011 |
| | Identification of genetic elements in metabolism by high-throughput mouse phenotyping | Q47643645 |
| | Highly-efficient, fluorescent, locus directed cre and FlpO deleter mice on a pure C57BL/6N genetic background. | Q50507031 |
| | Placentation defects are highly prevalent in embryonic lethal mouse mutants. | Q52726584 |
| | Animal-based studies will be essential for precision medicine. | Q52848545 |
| | Editing mammalian genomes: ethical considerations. | Q53194473 |
| | Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms. | Q55317074 |
| | The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation | Q57090269 |
| | No unexpected CRISPR-Cas9 off-target activity revealed by trio sequencing of gene-edited mice | Q89475108 |
| | The Deep Genome Project | Q89488064 |
| | Ensembl 2020 | Q91135329 |
| | Optimizing PCR for Mouse Genotyping: Recommendations for Reliable, Rapid, Cost Effective, Robust and Adaptable to High-Throughput Genotyping Protocol for Any Type of Mutation | Q91395278 |
| | CRISPResso2 provides accurate and rapid genome editing sequence analysis | Q91945589 |
| | New models for human disease from the International Mouse Phenotyping Consortium | Q92283778 |
| | Editing the Genome of Human Induced Pluripotent Stem Cells Using CRISPR/Cas9 Ribonucleoprotein Complexes | Q92620150 |
| | Common and distinct transcriptional signatures of mammalian embryonic lethality | Q93052863 |
| P4510 | describes a project that uses | massive parallel sequencing | Q6784807 |
| P577 | publication date | 2020-10-20 | |
| P1433 | published in | Methods | Q6823859 |
| P1476 | title | High-throughput genotyping of high-homology mutant mouse strains by next-generation sequencing | |