Клавиатура Hiper Genome GK-2 USB Black

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Игровая клавиатура HIPER GENOME GK-2 чёрная (104кл, USB, мембранная, RGB подсветка)

Клавиатура HIPER Genome GK-2 чёрная (104кл, USB, мембранная, RGB подсветка)

Клавиатура чёрная (104кл, USB, мембранная, RGB подсветка)

1610 RUR

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Игровая клавиатура HIPER GENOME GK-2 чёрная (104кл, USB, мембранная, RGB подсветка)

Бренд: HIPER; Модель: Genome GK-2; Назначение: настольный компьютер; Конструкция клавиатуры: классическая; Тип клавиатуры: мембранная; Цвета букв на клавишах: н/д; Материал корпуса клавиатуры: пластик; Цвет: черный; Игровая: да; Наличие подсветки: да; Наличие дисплея: нет; Подставка под запястья: Есть; Количество дополнительных клавиш: 3; Программируемые клавиши: 3 программируемых клавиши для макросов; Источник питания клавиатуры: от USB порта; Длина шнура: 1.5 м; Дополнительные возможности: подсветка клавиш клавиатуры, мультимедийная

1900 RUR

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Natalie Kuldell Genome Refactoring

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Genome editing - Wikipedia

Genome editing, or genome engineering, or gene editing, is a type of genetic engineering in which DNA is inserted, deleted, modified or replaced in the genome of a living organism. Unlike early genetic engineering techniques that randomly inserts genetic material into a host genome, genome editing targets the insertions to site specific locations.

Journal of Virology Journal Homepage

Lymphocytic choriomeningitis virus (LCMV) is a murine arenavirus whose glycoprotein consists of a transmembrane subunit (GP-2) and a receptor-binding subunit (GP-1). LCMV-neutralizing antibodies (nAbs) are directed against a single site on GP-1 and occur 1 month after the infection of cytotoxic-T-lymphocyte (CTL) deficient mice. In wild-type mice, however, CTLs control early infection, and ...

NCBI Genome Data Viewer

Genome Data Viewer. GDV supports the exploration and analysis of NCBI-annotated and selected non-NCBI annotated eukaryotic genome assemblies. Currently, over 1240 assemblies are available. Switch view. Search organisms. Filter assemblies. Downloads. Search in genome. To view more organisms in the tree, click on nodes that have '+' signs. Press and hold the '+' to expand and reveal all the ...

Genome-wide association study - Wikipedia

In genomics, a genome-wide association study (GWA study, or GWAS), also known as whole genome association study (WGA study, or WGAS), is an observational study of a genome-wide set of genetic variants in different individuals to see if any variant is associated with a trait. GWA studies typically focus on associations between single-nucleotide polymorphisms (SNPs) and traits like major human ...

Gene set enrichment analysis for genome-wide DNA ...

Law CW, Chen Y, Shi W, Smyth GK. voom: precision weights unlock linear model analysis tools for RNA-seq read counts. Genome Biol. 2014;15(2):R29. Article Google Scholar 61. Maksimovic J, Oshlack A, Phipson B. Gene set enrichment analysis for genome-wide DNA methylation data [Internet]. GitHub.

Cotton pan-genome retrieves the lost sequences and genes ...

Using pan-genome analyses, we identify 32,569 and 8851 non-reference genes lost from Gossypium hirsutum and Gossypium barbadense reference genomes respectively, of which 38.2% (39,278) and 14.2% (11,359) of genes exhibit presence/absence variation (PAV). We document the landscape of PAV selection accompanied by asymmetric gene gain and loss and identify 124 PAVs linked to favorable fiber ...

High-Throughput Sequencing Technologies

The human genome sequence has profoundly altered our understanding of biology, human diversity and disease. The path from the first draft sequence to our nascent era of personal genomes and genomic medicine has been made possible only because of the extraordinary advancements in DNA sequencing technologies over the past ten years. Here, we discuss commonly used high-throughput sequencing ...

How is the genome like an open book? New research shows ...

June 2, 2021 Source: New York University Summary: The organization of the human genome relies on physics of different states of matter - such as liquid and solid. The findings reveal how the ...

RSEM: accurate transcript quantification from RNA-Seq data ...

RNA-Seq is revolutionizing the way transcript abundances are measured. A key challenge in transcript quantification from RNA-Seq data is the handling of reads that map to multiple genes or isoforms. This issue is particularly important for quantification with de novo transcriptome assemblies in the absence of sequenced genomes, as it is difficult to determine which transcripts are isoforms of ...

Which of the following diseases is not caused by virus?(1 ...

GK Questions. Academic Questions. Biology Questions. Which Of The Following Diseases Is Not Caused By Virus 1 Mumps 2 Aids 3 Tuberculosis 4 Rabies. Which of the following diseases is not caused by virus?(1) Mumps(2) AIDS(3) Tuberculosis(4) Rabies . Answer: (3) Viruses cause the disease such as mumps, rabies, and AIDS. Tuberculosis is an infectious disease produced by the tuberculosis bacterium ...

GitHub - twbattaglia/RNAseq-workflow: A repository for ...

STAR outperforms other aligners by a factor of >50 in mapping speed, aligning to the human genome 550 million 2 × 76 bp paired-end reads per hour on a modest 12-core server, while at the same time improving alignment sensitivity and precision." The STAR aligner is a very fast and efficent spliced aligner tools for aligning RNAseq data to genomes. The STAR aligner has the capabilities to ...

mSystems Journal Homepage

Full-genome sequences of the first two SARS-CoV-2 viruses from India. Indian J Med Res 151:200–209. Crossref. PubMed. Google Scholar. 27. Tilocca B, Soggiu A, Sanguinetti M, Musella V, Britti D, Bonizzi L, Urbani A, Roncada P. 2020. Comparative computational analysis of SARS-CoV-2 nucleocapsid protein epitopes in taxonomically related coronaviruses. Microbes Infect 22:188–194. Crossref ...

Clonal Hematopoiesis and Risk of Atherosclerotic ...

In two retrospective case-control cohorts for the evaluation of early-onset myocardial infarction, participants with CHIP had a risk of myocardial infarction that was 4.0 times as great as in noncarriers (95% CI, 2.4 to 6.7). Mutations in DNMT3A, TET2, ASXL1, and JAK2 were each individually associated with coronary heart disease. CHIP carriers with these mutations also had increased coronary ...

Novel Morbillivirus as Putative Cause of Fetal Death and ...

A complete genome sequence of PoMV (GenBank accession no. MT511667) was obtained by using RT-PCR to fill the gap between the 2 contigs. We designed 14 pairs of primers according to the obtained genome sequence and sequenced the RT-PCR products again, confirming the accuracy of the whole-genome sequence. The genome size of PoMV is 15,714 bases and has a G+C content of 45.19%. The 3′ leader ...

MedlinePlus: Genetics

MedlinePlus Genetics provides information about the effects of genetic variation on human health. Learn about genetic conditions, genes, chromosomes, and more.

SPM - Statistical Parametric Mapping - FIL | UCL

Statistical Parametric Mapping Introduction. Statistical Parametric Mapping refers to the construction and assessment of spatially extended statistical processes used to test hypotheses about functional imaging data. These ideas have been instantiated in a free and open source software that is called SPM.. The SPM software package has been designed for the analysis of brain imaging data sequences.

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Клавиатура Defender GK-310L 45310

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Аксессуары для велосипедов и самокатов Puky Задняя корзина GK 2 для велосипеда Z2

Puky Задняя корзина GK 2 для велосипеда Z2 : аксессуар, который позволит вашему ребенку взять с собой в дорогу бутылочку воды и прочие необходимые предметы. Задняя корзина крепится на багажник велосипеда Puky Z2.

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Задняя корзина GK 2 для велосипеда Z2 Puky

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Matt Ridley Genome

Группа авторов Somatic Genome Variation

Written by an international team of experts, Somatic Genome Variation presents a timely summary of the latest understanding of somatic genome development and variation in plants, animals, and microorganisms. Wide-ranging in coverage, the authors provide an updated view of somatic genomes and genetic theories while also offering interpretations of somatic genome variation. The text provides geneticists, bioinformaticians, biologist, plant scientists, crop scientists, and microbiologists with a valuable overview of this fascinating field of research.

18941.14 RUR

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Группа авторов Whole Genome Amplification

Клавиатура Defender Doom Keeper GK-100DL 45100

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