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Hello there!

🧬 I am a soon to be finishing PhD Student at KTH working with omics method development and linked read sequencing.

🐍 I build Snakemake pipelines such as BLR.

I also contribute to several open source Python tools such as:

More about me:

Pontus Höjer's Projects

aquila icon aquila

Diploid personal genome assembly and comprehensive variant detection based on linked-reads

cue icon cue

Deep learning framework for SV calling and genotyping

ema icon ema

Fast & accurate alignment of barcoded short-reads

genetech icon genetech

material related to the genetech courses

hapcut2 icon hapcut2

software tools for haplotype assembly from sequence data

lrez icon lrez

Standalone tool and library allowing to work with barcoded linked-reads

misc icon misc

Collection of useful scripts

multiqc icon multiqc

Aggregate results from bioinformatics analyses across many samples into a single report.

naibr icon naibr

Novel Adjacency Identification with Barcoded Reads

novel-x icon novel-x

Novel insertion detection with 10X reads

pysam icon pysam

Pysam is a Python module for reading and manipulating SAM/BAM/VCF/BCF files. It's a lightweight wrapper of the htslib C-API, the same one that powers samtools, bcftools, and tabix.

samplot icon samplot

Plot structural variant signals from many BAMs and CRAMs

scg_lib_structs icon scg_lib_structs

Collections of library structure and sequence of popular single cell genomic methods

starcode icon starcode

All pairs search and sequence clustering

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