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RNA-seq03:21

RNA-seq

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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
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Updated: Jun 15, 2025

Sand Fly Phlebotomus papatasi Embryo Microinjection for CRISPR/Cas9 Mutagenesis
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Improved high quality sand fly assemblies enabled by ultra low input long read sequencing.

Michelle Huang1, Sarah Kingan2, Douglas Shoue1

  • 1Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA.

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|August 24, 2024
PubMed
Summary
This summary is machine-generated.

New high-quality reference genomes for Phlebotomus papatasi and Lutzomyia longipalpis sand flies were generated. These improved assemblies will advance research into leishmaniasis vector biology and epidemiology.

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Area of Science:

  • Genomics
  • Vector Biology
  • Tropical Diseases

Background:

  • Phlebotomine sand flies transmit leishmaniasis, a neglected tropical disease.
  • Previous reference genomes were limited, hindering high-resolution genomic studies of these disease vectors.

Purpose of the Study:

  • To generate updated, high-quality chromosome-level reference genome assemblies for two key leishmaniasis vectors: Phlebotomus papatasi and Lutzomyia longipalpis.
  • To provide enhanced genomic resources for understanding sand fly biology and leishmaniasis epidemiology.

Main Methods:

  • Utilized PacBio HiFi long-read sequencing and Hi-C technology.
  • Employed an ultra-low input library preparation protocol.
  • Generated chromosome-level assemblies for P. papatasi and Lu. longipalpis.

Main Results:

  • Achieved a 351.6 Mb assembly for P. papatasi with scaffold N50 of 111.8 Mb.
  • Achieved a 147.8 Mb assembly for Lu. longipalpis with scaffold N50 of 40.6 Mb.
  • BUSCO assessments confirmed high completeness of insecta orthologs (94.5% for P. papatasi, 95.6% for Lu. longipalpis).

Conclusions:

  • The new reference assemblies represent a significant improvement over previous versions.
  • These high-quality genomes will be crucial for future genomic research on phlebotomine sand flies and leishmaniasis.
  • Facilitates deeper insights into vector evolution and disease transmission dynamics.