Roald Forsberg

Publications8
h-index5
Citations87
Highly Influential Citations3
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Pollen grain size in four ploidy levels of genusAvena
SummaryPollen grain size in many genera positively correlated with chromosome number. In this study, oat (Avena) pollen grain size was examined in diploids (2×=14, one species, for accessions),… Expand
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Endosperm Balance Number and the polar-nuclei activation hypotheses for endosperm development in interspecific crosses of Solanaceae and Gramineae, respectively
The Endosperm Balance Number (EBN) and the polar-nuclei activation (PNA) hypotheses have been developed to interpret, explain and predict interspecific and interploidy crossabilities in the Solanums… Expand
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Discovery of 2n gametes in tetraploid oat Avena vaviloviana
SummarySexual polyploidization via the action of 2n gametes (gametes with the sporophytic chromosome number) has been identified as the most important evolutionary mode of polyploidization among… Expand
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C-banded karyotypes and meiotic abnormalities in germplasm derived from interploidy crosses in Avena
C-banded karyotypes of somatic chromosomes and meiotic abnormalities were investigated in four crown rust resistant lines derived from interploidy crosses in Avena.C-banding revealed that line… Expand
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A Computer Simulator for Assessing Different Challenges and Strategies of de Novo Sequence Assembly
TLDR
This study presents a new computer program for assessing the effects of different factors and sequencing strategies on de novo sequence assembly. Expand
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Abstract 5332: Comparison of variant calling from whole exome and transcriptome sequencing using CLC Cancer Research Workbench
The now commonplace application of whole exome and genome sequencing in cancer research and diagnostics has allowed for rapid identification of SNPs and InDels in protein coding regions, but neither… Expand
Abstract 4181: Accurate and fast detection and comparison of larger clinically relevant insertions and deletions
Larger somatic insertions and deletions in tumor samples are often of significant clinical impact. Many of them are cancer driver mutations and play an important role in drug treatment1. Detecting… Expand
Abstract 2227: An automatic pipeline to find and annotate rare subclonal somatic variants in a paired tumor/normal sample
Identifying and characterizing somatic variants in deep genome sequence data from tumor samples remains challenging and time-consuming. Of special interest in cancer research and diagnostics is the… Expand