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DiscoSnp++ : de novo detection of small variants from raw unassembled read set(s)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-642-16321-0_14openalex-snapshot
Identifying SNPs without a Reference Genome by Comparing Raw Reads
inferredcites →https://doi.org/10.1038/nature11632openalex-snapshot
An integrated map of genetic variation from 1,092 human genomes
inferredcites →https://doi.org/10.1038/nbt.2515openalex-snapshot
Mutation identification by direct comparison of whole-genome sequencing data from mutant and wild-type individuals using k-mers
inferredcites →https://doi.org/10.1038/ng.1028openalex-snapshot
De novo assembly and genotyping of variants using colored de Bruijn graphs
inferredcites →https://doi.org/10.1038/ng.3121openalex-snapshot
Comprehensive variation discovery in single human genomes
inferredcites →https://doi.org/10.1038/ng.806openalex-snapshot
A framework for variation discovery and genotyping using next-generation DNA sequencing data
inferredcites →https://doi.org/10.1038/nrg2986openalex-snapshot
Genotype and SNP calling from next-generation sequencing data
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/btr346openalex-snapshot
Paired-end RAD-seq forde novoassembly and marker design without available reference
inferredcites →https://doi.org/10.1093/bioinformatics/bts280openalex-snapshot
Exploring single-sample SNP and INDEL calling with whole-genomede novoassembly
inferredcites →https://doi.org/10.1093/bioinformatics/btt310openalex-snapshot
Informed and automated k -mer size selection for genome assembly
inferredcites →https://doi.org/10.1093/bioinformatics/btu406openalex-snapshot
GATB: Genome Assembly & Analysis Tool Box
inferredcites →https://doi.org/10.1093/bioinformatics/btv022openalex-snapshot
KMC 2: fast and resource-frugal k -mer counting
inferredcites →https://doi.org/10.1093/nar/gku1187openalex-snapshot
Reference-free detection of isolated SNPs
inferredcites →https://doi.org/10.1093/nar/gkw655openalex-snapshot
SNP calling from RNA-seq data without a reference genome: identification, quantification, differential analysis and impact on the protein sequence
inferredcites →https://doi.org/10.1093/nar/gni035openalex-snapshot
Simple and highly efficient BAC recombineering using galK selection
inferredcites →https://doi.org/10.1101/gr.2395204openalex-snapshot
De Novo Repeat Classification and Fragment Assembly
inferredcites →https://doi.org/10.1145/974614.974643openalex-snapshot
De novo repeat classification and fragment assembly
inferredcites →https://doi.org/10.1186/1748-7188-8-22openalex-snapshot
Space-efficient and exact de Bruijn graph representation based on a Bloom filter
inferredcites →https://doi.org/10.1186/2047-217x-1-18openalex-snapshot
SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler
inferredcites →https://doi.org/10.1371/journal.pgen.1003972openalex-snapshot
Whole Genome, Whole Population Sequencing Reveals That Loss of Signaling Networks Is the Major Adaptive Strategy in a Constant Environment
inferredcites →https://doi.org/10.1371/journal.pone.0060058openalex-snapshot
Identifying and Classifying Trait Linked Polymorphisms in Non-Reference Species by Walking Coloured de Bruijn Graphs
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ece3.6588openalex-snapshot
Investigating population‐scale allelic differential expression in wild populations of Oithona similis (Cyclopoida, Claus, 1866)
inferred← citeshttps://doi.org/10.1002/imt2.4openalex-snapshot
Applications of de Bruijn graphs in microbiome research
inferred← citeshttps://doi.org/10.1007/978-1-0716-2293-3_15openalex-snapshot
Alignment-Free Genotyping of Known Variations with MALVA
inferred← citeshttps://doi.org/10.1016/j.cels.2022.12.007openalex-snapshot
Pitfalls of genotyping microbial communities with rapidly growing genome collections
inferred← citeshttps://doi.org/10.1016/j.cub.2020.07.057openalex-snapshot
Identification of the First Oomycete Mating-type Locus Sequence in the Grapevine Downy Mildew Pathogen, Plasmopara viticola
inferred← citeshttps://doi.org/10.1016/j.isci.2019.07.011openalex-snapshot
MALVA: Genotyping by Mapping-free ALlele Detection of Known VAriants
inferred← citeshttps://doi.org/10.1016/j.isci.2019.07.032openalex-snapshot
Kevlar: A Mapping-Free Framework for Accurate Discovery of De Novo Variants
inferred← citeshttps://doi.org/10.1038/s41598-023-49462-xopenalex-snapshot
Identification and high-throughput genotyping of single nucleotide polymorphism markers in a non-model conifer (Abies nordmanniana (Steven) Spach)
inferred← citeshttps://doi.org/10.1093/aob/mcy113openalex-snapshot
Origin and parental genome characterization of the allotetraploidStylosanthes scabraVogel (Papilionoideae, Leguminosae), an important legume pasture crop
inferred← citeshttps://doi.org/10.1093/bioadv/vbab005openalex-snapshot
Comparative genome analysis using sample-specific string detection in accurate long reads
inferred← citeshttps://doi.org/10.1093/bioinformatics/btab790openalex-snapshot
Theory of local k-mer selection with applications to long-read alignment
inferred← citeshttps://doi.org/10.1093/gigascience/giaf061openalex-snapshot
PISAD: reference-free intraspecies sample anomalies detection tool based on k-mer counting
inferred← citeshttps://doi.org/10.1093/molbev/msaf077openalex-snapshot
Reference-Free Variant Calling with Local Graph Construction with ska lo (SKA)
inferred← citeshttps://doi.org/10.1093/nar/gkab025openalex-snapshot
Nebula: ultra-efficient mapping-free structural variant genotyper
inferred← citeshttps://doi.org/10.1093/nargab/lqab034openalex-snapshot
Hapo-G, haplotype-aware polishing of genome assemblies with accurate reads
inferred← citeshttps://doi.org/10.1101/2021.04.29.441957openalex-snapshot
How marine currents and environment shape plankton genomic differentiation: a mosaic view from Tara Oceans metagenomic data
inferred← citeshttps://doi.org/10.1101/2023.01.10.523380openalex-snapshot
The identification and analysis of meristematic mutations within the apple tree that developed the RubyMac sport mutation
inferred← citeshttps://doi.org/10.1101/2024.03.25.586631openalex-snapshot
Seamless, rapid and accurate analyses of outbreak genomic data using Split K-mer Analysis (SKA)
inferred← citeshttps://doi.org/10.1101/2025.07.08.663732openalex-snapshot
Identifying rare spontaneous mutations through wildtype E. coli population sequencing
inferred← citeshttps://doi.org/10.1101/599076openalex-snapshot
Linking Allele-Specific Expression And Natural Selection In Wild Populations
inferred← citeshttps://doi.org/10.1101/gr.279449.124openalex-snapshot
Seamless, rapid, and accurate analyses of outbreak genomic data using splitk-mer analysis
inferred← citeshttps://doi.org/10.1109/bibm49941.2020.9313433openalex-snapshot
Kmer2SNP: reference-free SNP calling from raw reads based on matching
inferred← citeshttps://doi.org/10.1111/1755-0998.12985openalex-snapshot
Discovering millions of plankton genomic markers from the Atlantic Ocean and the Mediterranean Sea
inferred← citeshttps://doi.org/10.1128/jcm.01842-22openalex-snapshot
In Silico Evaluation of Variant Calling Methods for Bacterial Whole-Genome Sequencing Assays
inferred← citeshttps://doi.org/10.1128/msphere.00482-19openalex-snapshot
Genomic Variation among Strains of Crithidia bombi and C. expoeki
inferred← citeshttps://doi.org/10.1186/s12859-020-03586-3openalex-snapshot
Variable-order reference-free variant discovery with the Burrows-Wheeler Transform
inferred← citeshttps://doi.org/10.1186/s12859-021-04018-6openalex-snapshot
Reliable genomic strategies for species classification of plant genetic resources
inferred← citeshttps://doi.org/10.1186/s12864-025-11722-7openalex-snapshot
A scalable distributed pipeline for reference-free variants calling
inferred← citeshttps://doi.org/10.1186/s12870-024-05628-xopenalex-snapshot
The identification and analysis of meristematic mutations within the apple tree that developed the RubyMac sport mutation
inferred← citeshttps://doi.org/10.1186/s13015-019-0137-8openalex-snapshot
SNPs detection by eBWT positional clustering
inferred← citeshttps://doi.org/10.1186/s13059-020-02244-4openalex-snapshot
Ratatosk: hybrid error correction of long reads enables accurate variant calling and assembly
inferred← citeshttps://doi.org/10.3389/fgene.2021.615958openalex-snapshot
Enabling Genomics Pipelines in Commodity Personal Computers With Flash Storage
inferred← citeshttps://doi.org/10.4230/lipics.wabi.2018.3openalex-snapshot
Detecting Mutations by eBWT
inferred← citeshttps://doi.org/10.64898/2025.12.01.691650openalex-snapshot
bronko: ultrafast, alignment-free detection of viral genome variation
inferred← citeshttps://doi.org/10.70675/2ccfc627z786ez4b47zae5ez4477d6c63f74openalex-snapshot
Le plancton épipélagique marin du point de vue de la génomique des populations : une étude moléculaire à travers les données métagénomiques et métatranscriptomiques issues des expéditions de Tara Oceans
inferred← citeshttps://doi.org/10.70675/c6735232zadb5z49f0z804dzddd24cdc8628openalex-snapshot
Transcriptome and genome analysis based on alignment-free protocols
inferred← citeshttps://doi.org/10.7717/peerj.9291openalex-snapshot
DiscoSnp-RAD: de novo detection of small variants for RAD-Seq population genomics
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