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Nature Biotechnology

Resumen/Descripción – provisto por la editorial en inglés
Nature Biotechnology is a monthly journal covering the science and business of biotechnology. It publishes new concepts in technology/methodology of relevance to the biological, biomedical, agricultural and environmental sciences as well as covers the commercial, political, ethical, legal, and societal aspects of this research. The first function is fulfilled by the peer-reviewed research section, the second by the expository efforts in the front of the journal. We provide researchers with news about business; we provide the business community with news about research developments.
Palabras clave – provistas por la editorial

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Disponibilidad
Institución detectada Período Navegá Descargá Solicitá
No detectada desde jul. 2012 / hasta dic. 2023 Nature.com

Información

Tipo de recurso:

revistas

ISSN impreso

1087-0156

ISSN electrónico

1546-1696

Editor responsable

Springer Nature

País de edición

Reino Unido

Fecha de publicación

Tabla de contenidos

How to grow (almost) anything: a hybrid distance learning model for global laboratory-based synthetic biology education

Eyal PerryORCID; Jessica Weber; Pat Pataranutaporn; Verena Volf; Laura Maria Gonzalez; Sara Nejad; Carolyn Angleton; Jia-En Chen; Ananda Gabo; Mani Sai Suryateja Jammalamadaka; Erkin Kuru; Patrick Fortuna; Andres RicoORCID; Karolina Sulich; Dominika Wawrzyniak; Joseph Jacobson; George Church; David Kong

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible

Exploring the value of a global gene drive project registry

Riley I. Taitingfong; Cynthia TriplettORCID; Váleri N. Vásquez; Ramya M. Rajagopalan; Robyn RabanORCID; Aaron RobertsORCID; Gerard Terradas; Bridget Baumgartner; Claudia Emerson; Fred Gould; Fredros Okumu; Cynthia E. Schairer; Hervé C. Bossin; Leah Buchman; Karl J. Campbell; Anna Clark; Jason DelborneORCID; Kevin EsveltORCID; Joshua Fisher; Robert M. Friedman; Gigi GronvallORCID; Nikos Gurfield; Elizabeth Heitman; Natalie Kofler; Todd KuikenORCID; Jennifer KuzmaORCID; Pablo Manrique-Saide; John M. MarshallORCID; Michael Montague; Amy C. Morrison; Chris C. Opesen; Ryan Phelan; Antoinette PiaggioORCID; Hector Quemada; Larisa Rudenko; Natéwindé Sawadogo; Robert SmithORCID; Holly Tuten; Anika Ullah; Adam Vorsino; Nikolai Windbichler; Omar S. AkbariORCID; Kanya LongORCID; James V. Lavery; Sam Weiss Evans; Karen Tountas; Cinnamon S. BlossORCID

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible

Multiplexed mapping of chromatin features at single-cell resolution

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible

Multimodal chromatin profiling using nanobody-based single-cell CUT&Tag

Marek BartosovicORCID; Gonçalo Castelo-BrancoORCID

<jats:title>Abstract</jats:title><jats:p>Probing histone modifications at a single-cell level in thousands of cells has been enabled by technologies such as single-cell CUT&amp;Tag. Here we describe nano-CUT&amp;Tag (nano-CT), which allows simultaneous mapping of up to three epigenomic modalities at single-cell resolution using nanobody-Tn5 fusion proteins. Multimodal nano-CT is compatible with starting materials as low as 25,000–200,000 cells and has significantly higher sensitivity and number of fragments per cell than single-cell CUT&amp;Tag. We use nano-CT to simultaneously profile chromatin accessibility, H3K27ac, and H3K27me3 in juvenile mouse brain, allowing for discrimination of more cell types and states than unimodal single-cell CUT&amp;Tag. We also infer chromatin velocity between assay for transposase-accessible chromatin (ATAC) and H3K27ac in the oligodendrocyte lineage and deconvolute H3K27me3 repressive states, finding two sequential waves of H3K27me3 repression at distinct gene modules during oligodendrocyte lineage progression. Given its high resolution, versatility, and multimodal features, nano-CT allows unique insights in epigenetic landscapes in complex biological systems at the single-cell level.</jats:p>

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible

Single-cell nanobody-based profiles of multiple epigenetic modalities and chromatin velocity

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible

Nanobody-tethered transposition enables multifactorial chromatin profiling at single-cell resolution

Tim StuartORCID; Stephanie Hao; Bingjie Zhang; Levan MekerishviliORCID; Dan A. LandauORCID; Silas ManiatisORCID; Rahul SatijaORCID; Ivan RaimondiORCID

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible

Illumina faces short-read rivals

Michael Eisenstein

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. 3-5

scChIX-seq infers dynamic relationships between histone modifications in single cells

Jake YeungORCID; Maria FlorescuORCID; Peter Zeller; Buys Anton de BarbansonORCID; Max D. Wellenstein; Alexander van OudenaardenORCID

<jats:title>Abstract</jats:title><jats:p>Regulation of chromatin states involves the dynamic interplay between different histone modifications to control gene expression. Recent advances have enabled mapping of histone marks in single cells, but most methods are constrained to profile only one histone mark per cell. Here, we present an integrated experimental and computational framework, scChIX-seq (single-cell chromatin immunocleavage and unmixing sequencing), to map several histone marks in single cells. scChIX-seq multiplexes two histone marks together in single cells, then computationally deconvolves the signal using training data from respective histone mark profiles. This framework learns the cell-type-specific correlation structure between histone marks, and therefore does not require a priori assumptions of their genomic distributions. Using scChIX-seq, we demonstrate multimodal analysis of histone marks in single cells across a range of mark combinations. Modeling dynamics of in vitro macrophage differentiation enables integrated analysis of chromatin velocity. Overall, scChIX-seq unlocks systematic interrogation of the interplay between histone modifications in single cells.</jats:p>

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible

Real-time monitoring of tumor-homing bacteria and tumor cells in vivo using ultrasound

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible

Writing cellular history in protein chains

Hyung-Bae KwonORCID

Palabras clave: Biomedical Engineering; Molecular Medicine; Applied Microbiology and Biotechnology; Bioengineering; Biotechnology.

Pp. No disponible