Karol Szlachta

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 5 papers. Top paper: “CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data”.

CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data

Genome biology(2020)10.1186/s13059-020-02043-x

N/A

0DataRank · unranked

120 citations

Yongjin Li, Michael N. Edmonson, Xin Zhou, Scott Newman, Clay McLeod +16 more

CNCC: an analysis tool to determine genome-wide DNA break end structure at single-nucleotide resolution

BMC Genomics(2020)10.1186/s12864-019-6436-0

N/A

0DataRank · unranked

13 citations

Heather M. Raimer, Laurey Comeau, Yuh‐Hwa Wang, Karol Szlachta

Topoisomerase II contributes to DNA secondary structure-mediated double-stranded breaks

Nucleic Acids Research(2020)10.1093/nar/gkaa483

N/A

0DataRank · unranked

41 citations

Arkadi Manukyan, Heather M. Raimer, Sandeep Singh, Anita Salamon, Wenying Guo +3 more

Pausing sites of RNA polymerase II on actively transcribed genes are enriched in DNA double-stranded breaks

Journal of Biological Chemistry(2020)10.1074/jbc.ra119.011665

N/A

0DataRank · unranked

39 citations

Karol Szlachta, Arkadi Manukyan, Heather M. Raimer, Manikarna Dinda, Stefan Bekiranov +2 more

SequencErr: measuring and suppressing sequencer errors in next-generation sequencing data

Genome biology(2021)10.1186/s13059-020-02254-2

N/A

0DataRank · unranked

73 citations

Yu Sun, Yanling Liu, Pandurang Kolekar, Ying Shao, Karol Szlachta +14 more