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References from UMI-Gen: A UMI-based read simulator for variant calling evaluation in paired-end sequencing NGS libraries. Local targets link to admitted publications; unresolved targets remain external evidence.
10.1073/pnas.1208715109
10.1073/pnas.1208715109 · External reference
10.1093/dnares/dsv010
10.1093/dnares/dsv010 · External reference
10.1038/nbt.3520
10.1038/nbt.3520 · External reference
Clonal haematopoiesis harbouring AML-associated mutations is ubiquitous in healthy adults
10.1038/ncomms12484 · 2016 · External reference
A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome
10.1136/jmedgenet-2016-104295 · 2017 · External reference
10.1109/tbme.2016.2560939
10.1109/tbme.2016.2560939 · External reference
SVSR: A program to simulate structural variations and generate sequencing reads for multiple platforms
10.1109/tcbb.2018.2876527 · 2020 · External reference
10.1093/bioinformatics/btw536
10.1093/bioinformatics/btw536 · External reference
10.18632/oncotarget.13103
10.18632/oncotarget.13103 · External reference
DeepSNVMiner: a sequence analysis tool to detect emergent, rare mutations in subsets of cell populations
10.7717/peerj.2074 · 2016 · External reference
UMI-VarCal: a new UMI-based variant caller that efficiently improves low-frequency variant detection in paired-end sequencing NGS libraries
10.1101/2020.04.22.027532 · 2020 · External reference
Illumina error profiles: resolving fine-scale variation in metagenomic sequencing data
10.1186/s12859-016-0976-y · 2016 · External reference
10.1101/gr.8.3.186
10.1101/gr.8.3.186 · External reference
10.1101/gr.8.3.175
10.1101/gr.8.3.175 · External reference
10.1093/bioinformatics/btp324
10.1093/bioinformatics/btp324 · External reference
10.1093/bioinformatics/btp352
10.1093/bioinformatics/btp352 · External reference
10.1038/nbt.1754
10.1038/nbt.1754 · External reference