These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
139 related articles for article (PubMed ID: 38717906)
1. Protocol for mapping physiological DSBs using in-suspension break labeling in situ and sequencing. Hidmi O; Oster S; Shatleh D; Monin J; Aqeilan RI STAR Protoc; 2024 Jun; 5(2):103059. PubMed ID: 38717906 [TBL] [Abstract][Full Text] [Related]
2. Genome-wide detection of DNA double-strand breaks by in-suspension BLISS. Bouwman BAM; Agostini F; Garnerone S; Petrosino G; Gothe HJ; Sayols S; Moor AE; Itzkovitz S; Bienko M; Roukos V; Crosetto N Nat Protoc; 2020 Dec; 15(12):3894-3941. PubMed ID: 33139954 [TBL] [Abstract][Full Text] [Related]
3. High-resolution, ultrasensitive and quantitative DNA double-strand break labeling in eukaryotic cells using i-BLESS. Biernacka A; Skrzypczak M; Zhu Y; Pasero P; Rowicka M; Ginalski K Nat Protoc; 2021 Feb; 16(2):1034-1061. PubMed ID: 33349705 [TBL] [Abstract][Full Text] [Related]
4. Genome-wide mapping of DNA double-strand breaks from eukaryotic cell cultures using Break-seq. Joshi I; DeRycke J; Palmowski M; LeSuer R; Feng W STAR Protoc; 2021 Jun; 2(2):100554. PubMed ID: 34189468 [TBL] [Abstract][Full Text] [Related]
5. Genome-Wide Profiling of DNA Double-Strand Breaks by the BLESS and BLISS Methods. Mirzazadeh R; Kallas T; Bienko M; Crosetto N Methods Mol Biol; 2018; 1672():167-194. PubMed ID: 29043625 [TBL] [Abstract][Full Text] [Related]
6. CNCC: an analysis tool to determine genome-wide DNA break end structure at single-nucleotide resolution. Szlachta K; Raimer HM; Comeau LD; Wang YH BMC Genomics; 2020 Jan; 21(1):25. PubMed ID: 31914926 [TBL] [Abstract][Full Text] [Related]
7. END-seq: An Unbiased, High-Resolution, and Genome-Wide Approach to Map DNA Double-Strand Breaks and Resection in Human Cells. Wong N; John S; Nussenzweig A; Canela A Methods Mol Biol; 2021; 2153():9-31. PubMed ID: 32840769 [TBL] [Abstract][Full Text] [Related]
8. Protocol for mapping double-stranded DNA break sites across the genome with translocation capture sequencing. Delaney JR; La Spada AR STAR Protoc; 2023 Mar; 4(2):102205. PubMed ID: 37000621 [TBL] [Abstract][Full Text] [Related]
9. An atlas of endogenous DNA double-strand breaks arising during human neural cell fate determination. Ballarino R; Bouwman BAM; Agostini F; Harbers L; Diekmann C; Wernersson E; Bienko M; Crosetto N Sci Data; 2022 Jul; 9(1):400. PubMed ID: 35821502 [TBL] [Abstract][Full Text] [Related]
10. Quantification of protein enrichment at site-specific DNA double-strand breaks by chromatin immunoprecipitation in cultured human cells. Sharma AK; Fitieh AM; Locke AJ; Ali JYH; Ismail IH STAR Protoc; 2023 Mar; 4(1):101917. PubMed ID: 36520630 [TBL] [Abstract][Full Text] [Related]
11. Nucleotide-resolution DNA double-strand break mapping by next-generation sequencing. Crosetto N; Mitra A; Silva MJ; Bienko M; Dojer N; Wang Q; Karaca E; Chiarle R; Skrzypczak M; Ginalski K; Pasero P; Rowicka M; Dikic I Nat Methods; 2013 Apr; 10(4):361-5. PubMed ID: 23503052 [TBL] [Abstract][Full Text] [Related]
12. Preparation and Analysis of GLOE-Seq Libraries for Genome-Wide Mapping of DNA Replication Patterns, Single-Strand Breaks, and Lesions. Petrosino G; Zilio N; Sriramachandran AM; Ulrich HD STAR Protoc; 2020 Sep; 1(2):100076. PubMed ID: 33111111 [TBL] [Abstract][Full Text] [Related]
13. qDSB-Seq is a general method for genome-wide quantification of DNA double-strand breaks using sequencing. Zhu Y; Biernacka A; Pardo B; Dojer N; Forey R; Skrzypczak M; Fongang B; Nde J; Yousefi R; Pasero P; Ginalski K; Rowicka M Nat Commun; 2019 May; 10(1):2313. PubMed ID: 31127121 [TBL] [Abstract][Full Text] [Related]
14. Protocol to measure end resection intermediates at sequence-specific DNA double-strand breaks by quantitative polymerase chain reaction using ER-AsiSI U2OS cells. Sharma AK; Fitieh AM; Hafez Ali JY; Ismail IH STAR Protoc; 2022 Dec; 3(4):101861. PubMed ID: 36595899 [TBL] [Abstract][Full Text] [Related]
15. PEM-seq comprehensively quantifies DNA repair outcomes during gene-editing and DSB repair. Liu Y; Yin J; Gan T; Liu M; Xin C; Zhang W; Hu J STAR Protoc; 2022 Mar; 3(1):101088. PubMed ID: 35462794 [TBL] [Abstract][Full Text] [Related]
16. Detecting RNA-protein proximity at DNA double-strand breaks using combined fluorescence in situ hybridization with proximity ligation assay. Alagia A; Ketley RF; Gullerova M STAR Protoc; 2023 Mar; 4(1):102096. PubMed ID: 36825808 [TBL] [Abstract][Full Text] [Related]
17. Mapping DNA Breaks by Next-Generation Sequencing. Baranello L; Kouzine F; Wojtowicz D; Cui K; Zhao K; Przytycka TM; Capranico G; Levens D Methods Mol Biol; 2018; 1672():155-166. PubMed ID: 29043624 [TBL] [Abstract][Full Text] [Related]
18. DSBCapture: in situ capture and sequencing of DNA breaks. Lensing SV; Marsico G; Hänsel-Hertsch R; Lam EY; Tannahill D; Balasubramanian S Nat Methods; 2016 Oct; 13(10):855-7. PubMed ID: 27525976 [TBL] [Abstract][Full Text] [Related]
19. Pausing sites of RNA polymerase II on actively transcribed genes are enriched in DNA double-stranded breaks. Singh S; Szlachta K; Manukyan A; Raimer HM; Dinda M; Bekiranov S; Wang YH J Biol Chem; 2020 Mar; 295(12):3990-4000. PubMed ID: 32029477 [TBL] [Abstract][Full Text] [Related]
20. The Landscape of Mouse Meiotic Double-Strand Break Formation, Processing, and Repair. Lange J; Yamada S; Tischfield SE; Pan J; Kim S; Zhu X; Socci ND; Jasin M; Keeney S Cell; 2016 Oct; 167(3):695-708.e16. PubMed ID: 27745971 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]