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Resolving within-host malaria parasite diversity using single-cell sequencing

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/j.ijpara.2007.05.003openalex-snapshot
Quantitative dissection of clone-specific growth rates in cultured malaria parasites
inferredcites →https://doi.org/10.1017/s0031182000059217openalex-snapshot
The epidemiology of multiple-clone Plasmodium falciparum infections in Gambian patients
inferredcites →https://doi.org/10.1038/nature01097openalex-snapshot
Genome sequence of the human malaria parasite Plasmodium falciparum
inferredcites →https://doi.org/10.1038/nature06954openalex-snapshot
Sex ratio adjustment and kin discrimination in malaria parasites
inferredcites →https://doi.org/10.1038/nature11174openalex-snapshot
Analysis of Plasmodium falciparum diversity in natural infections by deep sequencing
inferredcites →https://doi.org/10.1038/ng.3599openalex-snapshot
Genomic analysis of local variation and recent evolution in Plasmodium vivax
inferredcites →https://doi.org/10.1038/ng1924openalex-snapshot
Genome-wide variation and identification of vaccine targets in the Plasmodium falciparum genome
inferredcites →https://doi.org/10.1038/nm.2368openalex-snapshot
Host-mediated regulation of superinfection in malaria
inferredcites →https://doi.org/10.1038/nrg3187openalex-snapshot
Harnessing genomics and genome biology to understand malaria biology
inferredcites →https://doi.org/10.1038/s41467-018-03807-7openalex-snapshot
Host-mediated selection impacts the diversity of Plasmodium falciparum antigens within infections
inferredcites →https://doi.org/10.1073/pnas.0500078102openalex-snapshot
Virulence and competitive ability in genetically diverse malaria infections
inferredcites →https://doi.org/10.1073/pnas.0702715104openalex-snapshot
Population genetic structure of Plasmodium falciparum in the two main African vectors, Anopheles gambiae and Anopheles funestus
inferredcites →https://doi.org/10.1073/pnas.0707766104openalex-snapshot
Competitive release and facilitation of drug-resistant parasites after therapeutic chemotherapy in a rodent malaria model
inferredcites →https://doi.org/10.1093/bioinformatics/btu005openalex-snapshot
estMOI: estimating multiplicity of infection using parasite deep sequencing data
inferredcites →https://doi.org/10.1093/bioinformatics/btx145openalex-snapshot
SeqArray—a storage-efficient high-performance data format for WGS variant calls
inferredcites →https://doi.org/10.1093/bioinformatics/btx530openalex-snapshot
Deconvolution of multiple infections in Plasmodium falciparum from high throughput sequencing data
inferredcites →https://doi.org/10.1093/gbe/evx256openalex-snapshot
High-Resolution Single-Cell Sequencing of Malaria Parasites
inferredcites →https://doi.org/10.1098/rspb.2007.0873openalex-snapshot
Transmission stage investment of malaria parasites in response to in-host competition
inferredcites →https://doi.org/10.1098/rspb.2012.0113openalex-snapshot
Close kinship within multiple-genotype malaria parasite infections
inferredcites →https://doi.org/10.1101/gr.094052.109openalex-snapshot
Fast model-based estimation of ancestry in unrelated individuals
inferredcites →https://doi.org/10.1101/gr.115972.110openalex-snapshot
Maximum-likelihood estimation of recent shared ancestry (ERSA)
inferredcites →https://doi.org/10.1101/gr.168286.113openalex-snapshot
Single-cell genomics for dissection of complex malaria infections
inferredcites →https://doi.org/10.1101/gr.203711.115openalex-snapshot
Indels, structural variation, and recombination drive genomic diversity in Plasmodium falciparum
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01215.xopenalex-snapshot
WITHIN-HOST COMPETITION IN GENETICALLY DIVERSE MALARIA INFECTIONS: PARASITE VIRULENCE AND COMPETITIVE SUCCESS
inferredcites →https://doi.org/10.1126/science.7015505openalex-snapshot
Cloning of Naturally Occurring Mixed Infections of Malaria Parasites
inferredcites →https://doi.org/10.1186/1475-2875-11-380openalex-snapshot
Entomological indices of malaria transmission in Chikhwawa district, Southern Malawi
inferredcites →https://doi.org/10.1186/1475-2875-11-41openalex-snapshot
Using CF11 cellulose columns to inexpensively and effectively remove human DNA from Plasmodium falciparum-infected whole blood samples
inferredcites →https://doi.org/10.1186/1475-2875-14-4openalex-snapshot
COIL: a methodology for evaluating malarial complexity of infection using likelihood from single nucleotide polymorphism data
inferredcites →https://doi.org/10.1186/gb-2008-9-12-r171openalex-snapshot
Genome-wide SNP genotyping highlights the role of natural selection in Plasmodium falciparumpopulation divergence
inferredcites →https://doi.org/10.1186/gb-2011-12-4-r33openalex-snapshot
High recombination rates and hotspots in a Plasmodium falciparum genetic cross
inferredcites →https://doi.org/10.1186/s12936-018-2349-7openalex-snapshot
hmmIBD: software to infer pairwise identity by descent between haploid genotypes
inferredcites →https://doi.org/10.1186/s13073-017-0398-0openalex-snapshot
Genetic relatedness analysis reveals the cotransmission of genetically related Plasmodium falciparum parasites in Thiès, Senegal
inferredcites →https://doi.org/10.1371/journal.pbio.0030335openalex-snapshot
Recombination Hotspots and Population Structure in Plasmodium falciparum
inferredcites →https://doi.org/10.1371/journal.pcbi.1004824openalex-snapshot
Inferring Strain Mixture within Clinical Plasmodium falciparum Isolates from Genomic Sequence Data
inferredcites →https://doi.org/10.1371/journal.pcbi.1005348openalex-snapshot
THE REAL McCOIL: A method for the concurrent estimation of the complexity of infection and SNP allele frequency for malaria parasites
inferredcites →https://doi.org/10.1371/journal.pcbi.1005923openalex-snapshot
Modeling the genetic relatedness of Plasmodium falciparum parasites following meiotic recombination and cotransmission
inferredcites →https://doi.org/10.1371/journal.pgen.1004144openalex-snapshot
Relationship Estimation from Whole-Genome Sequence Data
inferredcites →https://doi.org/10.1371/journal.pgen.1007279openalex-snapshot
Identity-by-descent analyses for measuring population dynamics and selection in recombining pathogens
inferredcites →https://doi.org/10.1371/journal.pone.0032891openalex-snapshot
Characterization of Within-Host Plasmodium falciparum Diversity Using Next-Generation Sequence Data

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1021/acsinfecdis.9b00093openalex-snapshot
Post-Genomic Approaches to Understanding Malaria Parasite Biology: Linking Genes to Biological Functions
inferred← citeshttps://doi.org/10.1038/s41598-020-62819-wopenalex-snapshot
Diversity and Multiplicity of P. falciparum infections among asymptomatic school children in Mbita, Western Kenya
inferred← citeshttps://doi.org/10.1101/2023.03.06.531320openalex-snapshot
Antigenic strain diversity predicts different biogeographic patterns of maintenance and decline of anti-malarial drug resistance
inferred← citeshttps://doi.org/10.1101/793554openalex-snapshot
Evaluating the performance of malaria genomics for inferring changes in transmission intensity using transmission modelling
inferred← citeshttps://doi.org/10.1186/s12936-019-2880-1openalex-snapshot
Applying next-generation sequencing to track falciparum malaria in sub-Saharan Africa
inferred← citeshttps://doi.org/10.1186/s13073-021-00889-9openalex-snapshot
Single-cell sequencing of the small and AT-skewed genome of malaria parasites
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008453openalex-snapshot
Genetic mapping of fitness determinants across the malaria parasite Plasmodium falciparum life cycle
inferred← citeshttps://doi.org/10.1534/genetics.119.302120openalex-snapshot
Estimating Relatedness Between Malaria Parasites
inferred← citeshttps://doi.org/10.3390/biology11040587openalex-snapshot
Whole Genome Sequencing Contributions and Challenges in Disease Reduction Focused on Malaria
inferred← citeshttps://doi.org/10.7554/elife.90888openalex-snapshot
Antigenic strain diversity predicts different biogeographic patterns of maintenance and decline of antimalarial drug resistance
inferred← citeshttps://doi.org/10.7554/elife.90888.1openalex-snapshot
Antigenic strain diversity predicts different biogeographic patterns of invasion and maintenance of anti-malarial drug resistance
inferred← citeshttps://doi.org/10.7554/elife.90888.2openalex-snapshot
Antigenic strain diversity predicts different biogeographic patterns of maintenance and decline of anti-malarial drug resistance
inferred← citeshttps://doi.org/10.7554/elife.90888.3openalex-snapshot
Antigenic strain diversity predicts different biogeographic patterns of maintenance and decline of antimalarial drug resistance
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