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Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird

• Authors : Zhang, Hongkai; Lundberg, Max; Tarka, Maja ...

Subjects: Natural Sciences; Biological Sciences; Evolutionary Biology

• Source: Genome Biology and Evolution. 15(11)

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De novo mutations in children born after medical assisted reproduction

• Authors : Smits RM; Xavier MJ; Oud MS

• Source: Human Reproduction, 30 May 2022

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Genome-Wide Off-Target Analysis in CRISPR-Cas9 Modified Mice and Their Offspring

• Authors : Yan Dong; Haimei Li; Liang Zhao

Subjects: crispr-cas9; off-target; whole-genome sequencing

• Source: G3: Genes, Genomes, Genetics, Vol 9, Iss 11, Pp 3645-3651 (2019)

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Dog10K: an integrated Dog10K database summarizing canine multi-omics.

• Authors : Zhou T; Key Laboratory of Genetic Evolution & Animal Models, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan 650201, China.; Yunnan Key Laboratory of Molecular Biology of Domestic Animals, Chinese Academy of Sciences, Kunming, Yunnan 650201, China.

Subjects: Polymorphism, Single Nucleotide* ; Databases, Genetic*; Dogs/Dogs/Dogs/genetics

• Source: Nucleic acids research [Nucleic Acids Res] 2025 Jan 06; Vol. 53 (D1), pp. D939-D947.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium:

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DeNovoCNN: a deep learning approach to de novo variant calling in next generation sequencing data.

• Authors : Khazeeva G; Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Geert Grooteplein 10, 6525 GA Nijmegen, The Netherlands.; Sablauskas K

Subjects: Deep Learning* ; High-Throughput Nucleotide Sequencing*/High-Throughput Nucleotide Sequencing*/High-Throughput Nucleotide Sequencing*/methods; Sequence Analysis, DNA

• Source: Nucleic acids research [Nucleic Acids Res] 2022 Sep 23; Vol. 50 (17), pp. e97.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium:

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Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.

• Authors : Zhao G; National Clinical Research Centre for Geriatric Disorders, Department of Geriatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.

Subjects: Databases, Genetic* ; Genetic Predisposition to Disease* ; Molecular Sequence Annotation*

• Source: Nucleic acids research [Nucleic Acids Res] 2020 Jan 08; Vol. 48 (D1), pp. D913-D926.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium:

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EpiDenovo: a platform for linking regulatory de novo mutations to developmental epigenetics and diseases.

• Authors : Mao F; Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100101, China.; Department of Pathology, University of Michigan, Ann Arbor, MI 48109, USA.

Subjects: Databases, Genetic* ; Epigenesis, Genetic* ; Mutation*

• Source: Nucleic acids research [Nucleic Acids Res] 2018 Jan 04; Vol. 46 (D1), pp. D92-D99.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium:

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