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Search results for illumina pacbio
illumina
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14 search results found
Clair3
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191
Clair3 - Symphonizing pileup and full-alignment for high-performance long-read variant calling
Ampliseq
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141
Amplicon sequencing analysis workflow using DADA2 and QIIME2
Xtea
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70
Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics
Wengan
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57
An accurate and ultra-fast hybrid genome assembler
Mpgap
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51
Multi-platform genome assembly pipeline for Illumina, Nanopore and PacBio reads
Clairs
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42
ClairS - a deep-learning method for long-read somatic small variant calling
Awesome Sequencing Tech Papers
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26
A collection of publications on comparison of high-throughput sequencing technologies.
Ngs Preprocess
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23
A pipeline for preprocessing NGS data from Illumina, Nanopore and PacBio technologies
Clairs To
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18
ClairS-TO - a deep-learning method for tumor-only somatic SNV calling
Mgse
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16
Mapping-based Genome Size Estimation (MGSE) performs an estimation of a genome size based on a read mapping to an existing genome sequence assembly.
Fast Sg
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16
Fast-SG: An alignment-free algorithm for ultrafast scaffolding graph construction from short or long reads.
Sandy
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14
A straightforward and complete next-generation sequencing read simulator
Cliquesnv
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13
Kit4b
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5
A fully integrated K-mer Informed Toolkit for Bioinformatics
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1-14 of 14 search results
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