Top Tweets for #sequencedata
Improved Mutation Detection in Duplex Sequencing Data with Sample-Specific Error Profiles. #DuplexBasedVariantCalling #DataCorrection #SequenceData #ShorReads #Bioinformatics @biorxiv_bioinfo
https://t.co/R2Bn1wmOi6
GENOMICON-Seq enables realistic simulation of amplicon and exome sequencing for low-frequency mutation detection. #DataSimulation #SequenceData #LowFrequencyMutations #Bioinformatics #Genomics @SciReports
https://t.co/wTUegXIZmj
Haplotype-aware long-read error correction. #LongReads #SequenceData #ErrorCorrection #HaplotypeAware #Genomics #Bioinformatics @biorxiv_genomic
https://t.co/9xIul2QeYi
A new compression strategy to reduce the size of nanopore sequencing data. #DataCompression @nanopore #SequenceData #Bioinformatics #Genomics @genomeresearch
https://t.co/IHzUUHcHzY
We had an amazing time at @stambrosehigh on Monday with @4273pi, introducing #bioinformatics to brilliant @StAmbroseSci students! 🧬✨
Students looked at #sequencedata, used #BLAST, and analysed effects of #mutations!
@TheAmbeesHive #ScienceEducation #InspiringFutureScientists
altAFplotter: a web app for reliable UPD detection in NGS diagnostics. #UniparentalDisomies #SequenceData #Diagnostics @BMCBioinfo
https://t.co/tz1cn2LYn4
miniSNV: accurate and fast single nucleotide variant calling from nanopore sequencing data. #SNV #VariantCalling @nanopore #LongRead #SequenceData @BriefingBioinfo
https://t.co/a3bdpPwiCi
CleanUpRNAseq: An R/Bioconductor Package for Detecting and Correcting DNA Contamination in RNA-Seq Data. #RNAseq #SequenceData #DNAcontamination #BioTechJournal
https://t.co/tOvaVpHq1o
Benchmarking bacterial taxonomic classification using nanopore metagenomics data of several mock communities. #BacterialGenomes #Metagenomics #TaxonomicClassification @nanopore #SequenceData #Benchmarking @ScientificData
https://t.co/QeKIrU2Opl
SQANTI-reads: a tool for the quality assessment of long read data in multi-sample lrRNA-seq experiments. #LongReads #RNAseq #SequenceData #QualityAssessment @ConesaLab @biorxivpreprint https://t.co/ZZdJT5u3Ia
DeepBAM: a high-accuracy single-molecule CpG methylation detection tool for Oxford nanopore sequencing. #MethylationCallingMethod #MethylationCallsEvaluation #DeepNeuralNetworks #ModelImplementation @nanopore #SequenceData @BriefingBioinfo
https://t.co/KST5PqaYkc
LongReadSum: A fast and flexible quality control and signal summarization tool for long-read sequencing data. #LongRead #SequenceData #SequenceQC @biorxivpreprint
https://t.co/NVgdcgk5G9
SeqCAT: Sequence Conversion and Analysis Toolbox. #SequenceData #CoordinatesConversion #NGS #Bioinformatics @NAR_Open
https://t.co/KcG6qxuJ32
Bigtools: a high-performance BigWig and BigBed library in rust. #BigWig #BigBed #SequenceData #Rust #Bioinformatics
https://t.co/5pvlgAQKqx
PQSDC: a parallel lossless compressor for quality scores data via sequences partition and Run-Length prediction mapping. #SequenceData #FASTQfiles #DataCompression #QualityScores #Bioinformatics
https://t.co/TFqEAkGgd5
Streamlining remote nanopore data access with slow5curl. @nanopore #SequenceData @GigaScience
https://t.co/KbLf0BqGli
FMAlign2: a novel fast multiple nucleotide sequence alignment method for ultralong datasets. #SequenceAlignments #Ultralong #SequenceData #Bioinformatics
https://t.co/MRQNsJDWiP
HAT: de novo variant calling for highly accurate short-read and long-read sequencing data. #VariantCalling #LongReads #ShortReads #SequenceData #Bioinformatics
https://t.co/KfUaMJ62Vq
WFA-GPU: Gap-affine pairwise read-alignment using GPUs. #SequenceData #LongReads #ReadAlignment #Bioinformatics
https://t.co/g0kbquVkIp
MicrobeMod: A computational toolkit for identifying prokaryotic methylation and restriction-modification with nanopore sequencing. #BacterialGenomes #5mC #6mA #DNAmodifications #DataAnalysis #Bioinformatics @nanopore #SequenceData @biorxiv_bioinfo https://t.co/RuD2uROIhY
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