Dojer相关文献与解析，生知库 | 链接生命科学的每一步

qDSB-Seq is a general method for genome-wide quantification of DNA double-strand breaks using sequencing

qDSB-Seq 是一种利用测序对 DNA 双链断裂进行全基因组定量的通用方法

Yingjie Zhu, Anna Biernacka, Benjamin Pardo, Norbert Dojer, Romain Forey, Magdalena Skrzypczak, Bernard Fongang, Jules Nde, Razie Yousefi, Philippe Pasero, Krzysztof Ginalski, Maga Rowicka

发表日期：2019

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Comprehensive Mapping of Histone Modifications at DNA Double-Strand Breaks Deciphers Repair Pathway Chromatin Signatures

DNA 双链断裂处组蛋白修饰的综合映射可解释修复途径染色质特征

期刊:Molecular Cell

影响因子:14.5

doi:10.1016/j.molcel.2018.08.020

Thomas Clouaire, Vincent Rocher, Anahita Lashgari, Coline Arnould, Marion Aguirrebengoa, Anna Biernacka, Magdalena Skrzypczak, François Aymard, Bernard Fongang, Norbert Dojer, Jason S Iacovoni, Maga Rowicka, Krzysztof Ginalski, Jacques Côté, Gaëlle Legube

表观遗传

发表日期：2018

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Ssb1 and Ssb2 cooperate to regulate mouse hematopoietic stem and progenitor cells by resolving replicative stress

Ssb1 和 Ssb2 协同调节小鼠造血干细胞和祖细胞，以解决复制压力

期刊:Blood

影响因子:21

doi:10.1182/blood-2016-06-725093

Wei Shi, Therese Vu, Didier Boucher, Anna Biernacka, Jules Nde, Raj K Pandita, Jasmin Straube, Glen M Boyle, Fares Al-Ejeh, Purba Nag, Jessie Jeffery, Janelle L Harris, Amanda L Bain, Marta Grzelak, Magdalena Skrzypczak, Abhishek Mitra, Norbert Dojer, Nicola Crosetto, Nicole Cloonan, Olivier J Beche

Optimally choosing PWM motif databases and sequence scanning approaches based on ChIP-seq data

基于ChIP-seq数据优化选择PWM基序数据库和序列扫描方法

期刊:BMC Bioinformatics

影响因子:3.3

doi:10.1186/s12859-015-0573-5

Dabrowski, Michal; Dojer, Norbert; Krystkowiak, Izabella; Kaminska, Bozena; Wilczynski, Bartek

发表日期：2015

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RECORD: Reference-Assisted Genome Assembly for Closely Related Genomes

RECORD：参考基因组辅助组装近缘基因组

期刊:International Journal of Genomics

影响因子:1.9

doi:10.1155/2015/563482

Buza, Krisztian; Wilczynski, Bartek; Dojer, Norbert

发表日期：2015

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Nucleotide-resolution DNA double-strand break mapping by next-generation sequencing

通过下一代测序进行核苷酸分辨率 DNA 双链断裂图谱绘制

期刊:Nature Methods

影响因子:36.1

doi:10.1038/nmeth.2408

Nicola Crosetto, Abhishek Mitra, Maria Joao Silva, Magda Bienko, Norbert Dojer, Qi Wang, Elif Karaca, Roberto Chiarle, Magdalena Skrzypczak, Krzysztof Ginalski, Philippe Pasero, Maga Rowicka, Ivan Dikic

信号转导

发表日期：2013

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A probabilistic approach to learn chromatin architecture and accurate inference of the NF-κB/RelA regulatory network using ChIP-Seq

使用 ChIP-Seq 的概率方法来学习染色质结构并准确推断 NF-κB/RelA 调控网络

期刊:Nucleic Acids Research

影响因子:16.6

doi:10.1093/nar/gkt493

Jun Yang, Abhishek Mitra, Norbert Dojer, Shuhua Fu, Maga Rowicka, Allan R Brasier

AlfaPang: alignment free algorithm for pangenome graph construction

AlfaPang：一种无需比对即可构建泛基因组图的算法

Sequence Flow: interactive web application for visualizing partial order alignments

序列流：用于可视化部分序列比对的交互式网络应用程序

Getting insight into the pan-genome structure with PangTree

利用 PangTree 深入了解泛基因组结构

qDSB-Seq is a general method for genome-wide quantification of DNA double-strand breaks using sequencing

qDSB-Seq 是一种利用测序对 DNA 双链断裂进行全基因组定量的通用方法

Comprehensive Mapping of Histone Modifications at DNA Double-Strand Breaks Deciphers Repair Pathway Chromatin Signatures

DNA 双链断裂处组蛋白修饰的综合映射可解释修复途径染色质特征

Ssb1 and Ssb2 cooperate to regulate mouse hematopoietic stem and progenitor cells by resolving replicative stress

Ssb1 和 Ssb2 协同调节小鼠造血干细胞和祖细胞，以解决复制压力

Optimally choosing PWM motif databases and sequence scanning approaches based on ChIP-seq data

基于ChIP-seq数据优化选择PWM基序数据库和序列扫描方法

RECORD: Reference-Assisted Genome Assembly for Closely Related Genomes

RECORD：参考基因组辅助组装近缘基因组

Nucleotide-resolution DNA double-strand break mapping by next-generation sequencing

通过下一代测序进行核苷酸分辨率 DNA 双链断裂图谱绘制

A probabilistic approach to learn chromatin architecture and accurate inference of the NF-κB/RelA regulatory network using ChIP-Seq

使用 ChIP-Seq 的概率方法来学习染色质结构并准确推断 NF-κB/RelA 调控网络