30 Jun 2025
MetaGLIMPSE: Meta Imputation of Low Coverage Sequencing Data for Modern and Ancient Genomes. #GeneticImputation #LowCoverage #Sequencing #Genomics #Bioinformatics @biorxiv_genomic
biorxiv.org/content/10.1101/…
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17
1,009
Team visited door to door to mobilize people for RI vaccination and awareness in low coverage areas at East J.J Nagar Sub Center areas, under Kherengbar CHC, Belbari Block, West Tripura District.
#Awareness #mobilize #RI #lowcoverage
@USAID_MOMENTUM @JSIhealth @nhm_tripura
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9
84
South Team initiated Coordination Meeting with Frontline Health Workers about R.I Session's Importance in the low coverage areas, at Hrishyamukh CHC, under Hrishyamukh RD Block, South Tripura District.
#lowcoverage #RI #meeting #discussion
@USAID_MOMENTUM @JSIhealth @nhm_tripura
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12
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21 Jan 2023
KIN: a method to infer relatedness from low-coverage ancient DNA. #Relatedness #GeneticKinship #LowCoverage #SequenceData #AncientDNA @GenomeBiology
genomebiology.biomedcentral.…
2
260
17 Dec 2022
CONGA: Copy number variation genotyping in ancient genomes and low-coverage sequencing data. #CNV #AncientGenomes #LowCoverage #SequencingData #Bioinformatics @PLOSCompBiol
journals.plos.org/ploscompbi…
1
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768
5 Dec 2022
Accurate gene consensus at low nanopore coverage. #GeneConsensus @nanopore #LowCoverage #Sequencing #ErrorCorrection #Bioinformatics @GigaScience
academic.oup.com/gigascience…
11
33
27 Aug 2022
Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA. #WGS #LowCoverage #Sequencing #cfDNA @NatureComms
nature.com/articles/s41467-0…
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32
26 Aug 2022
Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA. #LowCoverage #WGS #cfDNA @naturecom
nature.com/articles/s41467-0…
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20
18 Jul 2022
Moment estimators of relatedness from low-depth whole-genome sequencing data. #Relatedness #Kinship #GenotypeData #LowCoverage @BMCBioinfo
bmcbioinformatics.biomedcent…
1
3
25 May 2022
Fast and accurate estimation of multidimensional site frequency spectra from low-coverage high-throughput sequencing data. #LowCoverage #Sequencing #AlleleFrequencies academic.oup.com/gigascience… @GigaScience
2
9 Apr 2022
A setback into a success: what can batch effects tell us about best practices in genomics? #BatchEffect #LowCoverage #NGS #Genomics
onlinelibrary.wiley.com/doi/… @molecology
1
11 Mar 2022
Gapless provides combined scaffolding, gap filling and assembly correction with long reads. #LongReads #LowCoverage #AssemblyCorrection #Scaffolding #GapFilling #Bioinformatics
biorxiv.org/content/10.1101/…
4
11
23 Dec 2021
CONGA: Copy number variation genotyping in ancient genomes and low-coverage sequencing data. #CNV #AncientGenomes #LowCoverage #SequencingData biorxiv.org/content/10.1101/… #Bioinformatics #Genomics
5
8
18 Dec 2021
VI Services
#LowNetwork
#LowSpeedNet
#LowCoverage
#LowCallQuality
Worst telecom company ever!
You can't even do your work, can't send data to anyone quickly, its uploading speed is not good nor downloading speed is good and its surfing speed either.
@ViCustomerCare
@TRAI
2
2
29 Oct 2021
LocalNgsRelate: a software tool for inferring IBD sharing along the genome between pairs of individuals from low-depth NGS data. #IBD #NGSdata #LowCoverage academic.oup.com/bioinformat… #Bioinformatics
2
3
15 Aug 2021
Powerful eQTL mapping through low coverage RNA sequencing. #eQTL #RNAseq #LowCoverage #BioInformatics biorxiv.org/content/10.1101/…
1
1
6 Apr 2020
Our pair of papers on the implementation of #lowcoverage sequencing coupled with hybrid peeling imputation in large pedigreed populations is out! With @AndrewCZWhalen @Vicky_CYCHEN @GregorGorjanc @woherring @alanjohnmileham @HickeyJohn @PigImprovement @Alpha_Genes ⬇️
2
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30 Oct 2019
New preprint on sequencing strategies best suited for pedigree-based imputation methods without reference panels. (Or how to use #lowcoverage in large populations!) With @AndrewCZWhalen @GregorGorjanc @alanjohnmileham @HickeyJohn @Alpha_Genes biorxiv.org/content/10.1101/…
1
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2 Aug 2019
#LowCoverage #WholeGenomeSequencing #lcWGS enables accurate assessment of common variants and calculation of genome-wide polygenic scores #GPS biorxiv.org/content/10.1101/…
2
Fast and efficient estimation of the nine condensed jacquard coefficients based on genotype likelihoods, which makes the method applicable to low-coverage sequencing data where it is not possible to call genotypes reliably. #ancientDNA #lowcoverage
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